40167812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52577309-G-A

40167854-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52577267-T-A

http://identifiers.org/hco/13/GRCh38#40167957-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52577159-C-A

40168095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52577028-C-T

40168107-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52577016-T-C

40168136-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52576986-T-G

40168200-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52576922-T-C

40168247-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52576876-A-G

40168286-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52576837-G-T

40168309-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52576816-T-A

40168978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52576026-T-C

40169027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52575964-G-A

40169027-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52575964-G-C

40169035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52575956-G-A

40169087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52575907-G-A

40169087-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52575907-G-C

http://identifiers.org/hco/13/GRCh38#40169089-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52575905-A-C

40169089-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52575905-A-T

40169442-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52575579-T-C

40169833-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52575225-T-G

40170826-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52573088-T-C

40170964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52572980-C-T

40171001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52572947-C-T

40172470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52570814-C-T

40172505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52570780-G-A

40172520-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52570768-T-C

40172562-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52570728-G-C

40172562-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52570728-G-T

40172736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52570583-C-T

http://identifiers.org/hco/13/GRCh38#40172873-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52570463-C-A

40172972-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52570367-G-T

40173156-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52570129-T-A

40173590-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52569718-A-G

40173731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52569561-G-A

40173738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52569554-C-T

http://identifiers.org/hco/13/GRCh38#40173974-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52569023-A-C

40174172-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52568847-T-G

40174383-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52568631-T-G

40174531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52568486-G-A

40174651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52568359-C-T

40174691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52568326-G-A

40175093-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52568065-G-T

40175231-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52567951-T-G

40175260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52567922-C-T

40175333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52567851-G-A

40175521-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52567699-A-G

40175676-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52567614-A-T

40175709-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52567581-T-C

40175910-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52567344-A-T

http://identifiers.org/hco/13/GRCh38#40175911-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52567343-C-A

40175911-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52567343-C-G

40176030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52567232-C-T

40176360-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52566952-C-G

40176443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52566879-G-A

40176492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52566825-C-T

40177687-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52566076-C-G

40177687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52566076-C-T

40177794-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52565978-T-C

40177919-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52565845-G-A

40177969-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52565784-C-G

40178242-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52565515-T-C

40178428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52565342-G-A

40178480-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52563748-C-G

40178529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52563700-C-T

40178588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52563638-T-C

40179591-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52562974-A-G

40180112-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52562451-A-G

40180127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52562434-C-T

40180267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52562297-C-T

40180282-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52562282-T-C

40180583-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52561987-T-G

40180824-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52561778-T-A

40181060-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52561544-C-G

40181060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52561544-C-T

40181104-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52561506-T-A

40181222-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52561232-T-G

40181276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52561177-C-T

40181559-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 52560743-A-T

40181588-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 52560722-C-G

40181588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 52560722-C-T

40181844-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 52560471-A-T

http://identifiers.org/hco/13/GRCh38#40182536-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52559805-C-A

40182555-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52559790-T-C

40182871-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52559491-T-G

40183064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52559299-A-G

40183503-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52558834-T-G

40183731-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52558275-G-T

40183802-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52558206-T-A

40183851-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52558154-T-C

40184384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52557654-G-A

40184399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52557639-C-T

40184447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52557593-G-A

40184545-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52557486-C-G

http://identifiers.org/hco/13/GRCh38#40184780-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52557267-C-A

40184780-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52557267-C-G

40184780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52557267-C-T

40185184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52556852-T-C

http://identifiers.org/hco/13/GRCh38#40185243-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52556794-A-C

http://identifiers.org/hco/13/GRCh38#40185313-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52556727-A-C

http://identifiers.org/hco/13/GRCh38#40185466-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52556584-C-A

40186766-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52556495-G-T

http://identifiers.org/hco/13/GRCh38#40186775-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52556486-C-A

40186806-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52556455-G-T

40186850-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52556414-T-A

40186946-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52556318-G-T

40186989-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52556275-A-T

40187670-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52555214-T-A

40187670-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52555214-T-G

40187754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52555148-T-C

40187816-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52555086-G-A

40187823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52555080-C-T

40187838-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52555065-G-T

40187842-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52555061-A-G

40187901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52555016-G-A

40187933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52554988-T-C

40187978-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52554959-A-G

40187978-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52554959-A-T

http://identifiers.org/hco/13/GRCh38#40187994-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52554948-C-A

40187994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52554948-C-T

http://identifiers.org/hco/13/GRCh38#40188051-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52554890-C-A

40188051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52554890-C-T

40188069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52554873-G-A

40188074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52554868-A-G

40188098-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52554845-G-T

40188108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52554835-C-T

40188191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52554750-G-A

40188332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52554613-C-T

40188419-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52554492-C-G

40188419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52554492-C-T

http://identifiers.org/hco/13/GRCh38#40188534-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52554389-C-A

40188534-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52554389-C-T

40188599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52554343-C-T

40188628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52554329-G-A

40188628-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52554329-G-T

40188732-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52554228-A-T

http://identifiers.org/hco/13/GRCh38#40188749-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52554211-C-A

http://identifiers.org/hco/13/GRCh38#40188767-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52554193-C-A

40188767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52554193-C-T

40188782-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52554178-T-C

40188793-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52554167-T-C

40188814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52554148-G-A

40188814-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52554148-G-T

40188978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52554032-G-A

40189000-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52554010-T-C

40189026-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52553985-A-G

40189037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52553974-G-A

40189559-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52552802-A-T

40189699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52552670-G-A

40189705-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52552658-A-G

40189720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52552643-G-A

40189806-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52552564-A-G

40189973-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52552446-T-C

40190154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52552256-G-A

40190181-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52552229-T-A

40190270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52552115-G-A

40191020-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52551356-T-C

40191021-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52551355-A-G

40191026-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52551350-G-C

40191032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52551345-C-T

40191201-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52551180-A-G

40191576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52550817-C-T

40191961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52550429-G-A

40192154-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52550239-A-T

40192458-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52549948-G-T

40192540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52549869-T-C

40192632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52549784-G-A

40192671-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52549755-C-G

40192801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52549632-G-A

40192880-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52549552-G-T

40192930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52549495-G-A

40193235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52549250-A-G

40193396-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52549086-T-A

40193516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52548967-C-T

40193586-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52548902-A-G

40193612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52548874-G-A

40194006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52548494-G-A

http://identifiers.org/hco/13/GRCh38#40194126-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52548364-A-C

40194171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52548328-T-C

40194171-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52548328-T-G

40194483-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52548040-T-C

40194595-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52547917-A-G

40194653-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52547875-G-T

http://identifiers.org/hco/13/GRCh38#40194735-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52547798-C-A

40194767-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52547768-T-C

40194769-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52547766-G-T

40194803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52547733-C-T

40195909-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52547643-G-T

40195929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52547623-G-A

http://identifiers.org/hco/13/GRCh38#40195991-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52547562-C-A

40196012-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52547541-T-C

40196075-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52547476-G-T

40196082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52547469-G-A

40196096-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52547455-G-C

40196096-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52547455-G-T

40196232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52547328-G-A

40196408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52547160-C-T

40196441-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52547131-A-G

http://identifiers.org/hco/13/GRCh38#40196462-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52547110-C-A

40196490-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52547083-A-G

http://identifiers.org/hco/13/GRCh38#40196999-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52546569-C-A

40197070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52546499-G-A

http://identifiers.org/hco/13/GRCh38#40197191-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52546404-C-A

40197324-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52546289-A-G

40197327-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52546286-G-T

40197367-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52546247-G-T

40197396-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52546218-G-T

40197421-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52546193-G-T

http://identifiers.org/hco/13/GRCh38#40197453-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52546160-C-A

40197458-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52546155-T-C

http://identifiers.org/hco/13/GRCh38#40197536-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52546091-C-A

40197658-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52545977-A-G

40197658-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52545977-A-T

40197734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52545928-G-A

40197734-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52545928-G-T

40197826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52545829-G-A

40197826-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52545829-G-T

40197872-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52545783-G-T

40197874-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52545781-T-C

40198597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52545665-C-T

40198625-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52545637-T-C

40198634-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52545631-A-G

40198739-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52545557-A-T

40198827-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52545490-T-A

http://identifiers.org/hco/13/GRCh38#40198831-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52545486-C-A

40198893-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52545453-T-C

http://identifiers.org/hco/13/GRCh38#40198944-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52545402-C-A

40198944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52545402-C-T

http://identifiers.org/hco/13/GRCh38#40198962-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52545384-A-C

40199306-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52545352-T-A

40199306-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52545352-T-C

40199306-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52545352-T-G

40199514-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52545086-T-C

40199579-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52545020-T-C

40199884-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52544837-C-G

40199951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52544781-C-T

http://identifiers.org/hco/13/GRCh38#40199978-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52544754-C-A

40200117-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52544617-T-A

40200458-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52544302-G-T

40200473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52544287-C-T

40200500-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52544261-T-C

40200712-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52544085-G-C

40200712-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52544085-G-T

40200849-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52543949-T-C

40200865-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52543919-T-C

http://identifiers.org/hco/13/GRCh38#40200915-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52543388-C-A

40200942-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52543365-T-G

40200949-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52543358-G-T

40201096-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52543226-A-G

40201244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52543095-C-T

40201567-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52542182-G-T

40201670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52542081-G-A

40203022-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52540980-T-C

40203032-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52540970-T-C

40203048-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52540954-G-C

40203116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52540897-G-A

40203689-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52540742-A-T

http://identifiers.org/hco/13/GRCh38#40203726-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52540702-C-A

40203791-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52540644-G-T

40203820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52540615-C-T

http://identifiers.org/hco/13/GRCh38#40203881-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52540474-C-A

40203933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52540420-T-C

40204239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52540152-C-T

40204395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52540014-C-T

40205765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52539336-A-G

40205899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52539201-C-T

40205948-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52539152-A-T

40206097-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52538983-G-T

40206183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52538896-G-A

40206183-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52538896-G-T

40206276-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52538804-T-A

http://identifiers.org/hco/13/GRCh38#40206367-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52538713-A-C

http://identifiers.org/hco/13/GRCh38#40206373-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52538707-C-A

http://identifiers.org/hco/13/GRCh38#40206451-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52538634-A-C

40206451-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52538634-A-G

40206455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52538630-T-C

40206496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52538589-C-T

40206534-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52538557-T-A

40206572-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52538520-G-T

http://identifiers.org/hco/13/GRCh38#40206812-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52538327-C-A

40206822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52538316-A-G

http://identifiers.org/hco/13/GRCh38#40206826-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52538312-C-A

40206879-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52538272-A-G

40206915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52538212-C-T

40207103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52538009-G-A

40207103-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52538009-G-T

40207172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52537950-G-A

40207177-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52537945-A-G

40207177-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52537945-A-T

http://identifiers.org/hco/13/GRCh38#40207194-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#52537929-C-A

40207421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52537738-C-T

40207653-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52537535-G-A

http://identifiers.org/hco/13/GRCh38#40207725-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52537482-C-A

40207725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52537482-C-T

40207814-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52537396-A-G

40207921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52537291-C-T

40207934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52537278-C-T

40207950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52537262-C-T

40208065-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52537140-T-C

40208065-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52537140-T-G

40208198-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52536997-T-C

40208219-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52536976-G-T

40208362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52535465-G-A

40208523-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52535321-T-C

http://identifiers.org/hco/13/GRCh38#40208586-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52535259-C-A

40208636-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52535214-C-T

40208657-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52535191-C-G

40208657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52535191-C-T

40208660-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52535188-A-T

40208994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52534932-G-A

40209245-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52534714-T-C

40209263-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52534696-C-G

40209588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52534370-G-A

40209835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52534113-C-T

40209910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52534044-C-T

40210543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52533769-G-A

40210618-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52533692-T-C

40210765-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52533555-T-C

40210833-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52533497-A-G

40210974-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52533372-T-C

40213473-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52532985-T-A

http://identifiers.org/hco/13/GRCh38#40213548-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52532914-A-C

40213548-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52532914-A-G

40213873-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52532585-A-G

40213934-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52532532-G-C

http://identifiers.org/hco/13/GRCh38#40214012-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52532459-C-A

40214012-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52532459-C-G

http://identifiers.org/hco/13/GRCh38#40214095-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52532392-A-C

40214128-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52532359-T-A

40214128-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52532359-T-C

40215396-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52531328-T-A

http://identifiers.org/hco/13/GRCh38#40215406-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52531318-A-C

40215458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52531279-A-G

http://identifiers.org/hco/13/GRCh38#40215634-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52531088-A-C

40215634-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52531088-A-G

40216240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52530530-C-T

40216401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52530393-C-T

http://identifiers.org/hco/13/GRCh38#40216503-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52530317-A-C

40216503-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52530317-A-T

http://identifiers.org/hco/13/GRCh38#40216537-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52530282-C-A

40216537-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52530282-C-T

40216706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52530065-G-A

40217914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52529577-G-A

40218099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52529401-C-T

40218500-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52528218-G-C

40218968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52527760-A-G

http://identifiers.org/hco/13/GRCh38#40220039-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52526339-C-A

40220234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52526157-C-T

40220255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52526042-G-A

40220287-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52526004-T-C

40220352-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52525943-G-T

http://identifiers.org/hco/13/GRCh38#40220430-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52525869-C-A

40220430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 52525869-C-T

http://identifiers.org/hco/13/GRCh38#40220438-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52525861-C-A

40220438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 52525861-C-T

40220616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52525686-T-C

40220721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52525566-G-A

40221260-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52525283-G-C

http://identifiers.org/hco/13/GRCh38#40221338-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52525202-A-C

40221776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52524798-G-A

40221783-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52524791-T-G

40221836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52524743-G-A

40221866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52524713-G-A

40222287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52524157-G-A

40222287-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52524157-G-T

40222301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52524144-A-G

40222324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52524124-G-A

40222439-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52524025-T-C

40222455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52524010-C-T

40222479-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52523986-T-G

40222856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52523069-T-C

40222896-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52523046-T-C

40223017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52522936-C-T

40223106-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52522865-A-G

40223171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52522588-G-A

40223244-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52522522-T-A

40223329-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52522441-G-C

40223738-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52522112-T-C

40223743-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52522107-G-C

40223985-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52521913-G-C

40223995-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52521903-T-C

http://identifiers.org/hco/13/GRCh38#40224436-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52521540-C-A

40227749-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52519732-T-C

40227753-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52519728-T-A

40227768-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52519713-G-T

40228180-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52519325-A-G

40228261-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52519237-T-A

40228266-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52519232-A-T

40228822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52518671-G-A

40229236-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52518368-T-A

40229618-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52518003-G-C

40229618-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52518003-G-T

40229707-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52517930-T-C

40229721-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52517874-A-T

40229747-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52517848-T-A

40229747-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52517848-T-C

40229766-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52517829-A-G

40229817-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52517806-T-A

40229817-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52517806-T-C

40229852-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52517771-A-T

40229854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52517769-T-C

40229854-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52517769-T-G

40229862-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52517761-T-A

http://identifiers.org/hco/13/GRCh38#40229912-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52517720-C-A

40230000-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52517674-A-G

40230001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52517673-C-T

40230990-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52515585-G-C

40231390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52515201-C-T

40231495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52515116-G-A

40232129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52514496-T-C

40232885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52512644-G-A

40232916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52512614-G-A

40233029-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52512505-T-C

40233505-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52511290-C-G

40233505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52511290-C-T

40233596-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52511213-A-G

40233613-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52511196-A-T

40233789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52510995-G-A

40233897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52510888-C-T

40234106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52510722-C-T

40234190-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52510640-T-C

40234358-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52510463-G-C

http://identifiers.org/hco/13/GRCh38#40234488-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52510305-C-A

40234488-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52510305-C-G

40234894-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52510202-T-A

40235393-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52509641-A-G

40235679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52509362-G-A

40236360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52508679-T-C

40236704-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52508336-T-G

40236819-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52508215-G-T

40237014-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52508020-G-T

40237069-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52507966-T-A

40237827-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52507339-T-C

40238005-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52506777-G-T

40238222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52506586-T-C

40238348-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52506481-G-C

40238401-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52506433-G-C

http://identifiers.org/hco/13/GRCh38#40238554-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52506267-A-C

40238604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52506225-C-T

http://identifiers.org/hco/13/GRCh38#40238783-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52506039-C-A

40238862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52505960-G-A

40238862-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52505960-G-T

40238958-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52505888-C-G

40238995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52505852-G-A

40239039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52505803-A-G

40239311-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52505585-T-G

40239339-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52505558-G-T

40239341-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52505556-G-T

40239408-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52505512-T-C

40239548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52505374-G-A

http://identifiers.org/hco/13/GRCh38#40239562-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52505360-A-C

40239665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52505264-A-G

40239669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52505260-G-A

40239699-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52505234-T-C

40239818-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52505120-A-G

40239818-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52505120-A-T

40239851-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52505091-A-G

40240095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52504856-C-T

40240328-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52504662-A-G

http://identifiers.org/hco/13/GRCh38#40240399-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52504592-A-C

40240399-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52504592-A-G

40240993-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52503973-C-G

40240993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52503973-C-T

40241551-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52503137-T-G

40243405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52502530-C-T

40243521-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52502392-A-G

40243935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52501979-G-A

http://identifiers.org/hco/13/GRCh38#40244003-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52501912-A-C

40244003-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52501912-A-G

40244036-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52501879-A-G

http://identifiers.org/hco/13/GRCh38#40244315-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52501682-C-A

40244315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52501682-C-T

40244636-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52501403-T-A

40252551-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52497935-T-C

40252551-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52497935-T-G

40252555-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52497931-T-C

40252889-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52497606-G-T

40253107-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52497387-A-G

40253125-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52497372-A-T

40253195-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52497327-A-G

40253224-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52497299-T-C

40254823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52495733-G-A

40259008-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52493809-T-C

40259258-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52493575-G-C

40259302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52493533-C-T

40259331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52493504-A-G

http://identifiers.org/hco/13/GRCh38#40259446-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52493415-A-C

40259452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52493409-C-T

40259514-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52493353-T-C

40259854-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52492863-G-T

40259945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52492575-G-A

40259991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52492529-C-T

40260037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52492474-A-G

40260245-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52492279-T-G

40260327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52492209-G-A

40261073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52491708-G-A

40261157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52491685-G-A

40261168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52491674-C-T

40261187-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52491647-T-C

40261204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52491632-G-A

40261251-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52491587-A-T

40261309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52491528-A-G

40261565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52491196-C-T

40261656-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52491105-T-A

40261656-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52491105-T-C

40261733-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52490624-G-T

40262092-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52490182-A-G

40262096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52490178-G-A

40262109-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52490165-T-C

40262112-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52490162-A-G

40262113-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52490161-T-C

40262117-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52490157-T-C

40262121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52490153-T-C

40262133-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52490081-T-A

40262133-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52490081-T-C

40262149-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52490065-T-A

http://identifiers.org/hco/13/GRCh38#40262217-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52489781-C-A

40262418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52489568-G-A

40262623-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52489445-C-G

40262729-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52489331-A-T

40262764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52489295-G-A

40262970-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52489096-A-G

40263000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52489072-C-T

40267131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52487849-G-A

http://identifiers.org/hco/13/GRCh38#40267171-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52487805-C-A

40267171-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52487805-C-G

40267171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52487805-C-T

40267258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52487703-C-T

40267339-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52487627-G-T

40267363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52487587-C-T

40267544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52487413-G-A

40267544-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52487413-G-C

40267651-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52487335-A-G

40267694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52487305-A-G

40267972-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52487021-G-C

40268083-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52486921-T-G

40268343-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52486619-T-C

40268590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52486348-G-A

http://identifiers.org/hco/13/GRCh38#40268609-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52486329-A-C

40268947-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52486028-T-C

40269035-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52485939-G-C

40269234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52485772-G-A

40269452-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52485539-C-G

40269452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52485539-C-T

40271630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52484954-G-A

40271789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52484883-G-A

40271805-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52484870-T-C

40271807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52484868-T-C

40272162-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52484540-T-A

40272162-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52484540-T-C

40272674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52484020-A-G

40272681-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52484013-A-G

40273508-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52483147-A-G

http://identifiers.org/hco/13/GRCh38#40273645-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52482958-C-A

40273797-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52482807-G-C

40274000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52482604-G-A

http://identifiers.org/hco/13/GRCh38#40274031-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52482574-C-A

40274298-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52482327-T-C

40274491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52482153-G-A

40274497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52482147-G-A

40274497-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52482147-G-T

40274728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52481945-G-A

40274981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52481699-C-T

40276296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52481454-G-A

40276420-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52481334-G-A

40276421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52481333-G-A

40276733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52480868-C-T

40276774-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52480827-G-C

40276785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52480821-C-T

40278993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52479749-G-A

40279542-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52479639-A-G

http://identifiers.org/hco/13/GRCh38#40279804-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52479407-C-A

40279804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52479407-C-T

40279822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52479391-A-G

40279852-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52479361-A-G

40279859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52479353-G-A

40279892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52479322-C-T

40283016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52477663-G-A

40283235-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52477431-T-A

40283245-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52477404-T-A

http://identifiers.org/hco/13/GRCh38#40283302-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52477332-C-A

40283621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52476817-C-T

40283675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52476774-C-T

40283791-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52476685-A-G

40283810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52476666-G-A

40283944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52476542-C-T

40284820-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52476027-T-A

40284820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52476027-T-C

40284924-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52475861-T-A

40284988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52475796-T-C

40285060-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52475696-G-T

40285062-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52475694-A-G

40285071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52475691-T-C

40285316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52475461-G-A

40285394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52475384-G-A

40285396-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52475382-C-G

40285425-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52475351-T-C

40285488-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52475288-A-G

40285518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52475258-C-T

40291022-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52474950-T-A

40291022-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52474950-T-C

http://identifiers.org/hco/13/GRCh38#40291072-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52474902-C-A

40291376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52474602-G-A

40291573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52474429-C-T

40291583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52474418-A-G

40293059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52471370-G-A

40293250-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52471199-G-C

40294435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52470957-G-A

40294561-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52470731-T-C

40295159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52470140-G-A

40295181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52470118-C-T

http://identifiers.org/hco/13/GRCh38#40295216-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52470083-C-A

40295218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52470081-G-A

40295324-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52469984-C-G

40295345-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52469969-T-C

http://identifiers.org/hco/13/GRCh38#40295603-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52469736-C-A

40309958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52468831-C-T

40310252-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52468559-G-C

40310428-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52468088-A-G

40310443-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52468073-T-A

40310443-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52468073-T-C

40310553-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52467935-G-T

40310582-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52467913-A-G

40310675-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52467825-A-T

40310819-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52467702-T-C

http://identifiers.org/hco/13/GRCh38#40310855-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52467666-A-C

40310954-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52467571-T-C

http://identifiers.org/hco/13/GRCh38#40311035-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52467469-C-A

40311035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52467469-C-T

40311085-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52467424-T-A

40311113-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52467403-T-C

40311223-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52467308-A-G

40311252-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52467274-G-T

40311576-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52466778-T-C

40311608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52466749-G-A

40311653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52466705-C-T

40311738-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52466617-T-A

40311927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52466426-C-T

40312000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52466345-C-T

http://identifiers.org/hco/13/GRCh38#40312078-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52466264-C-A

40312218-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52466152-T-A

40312218-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52466152-T-C

40312348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52466021-A-G

40312405-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52465963-G-T

40312790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52465668-C-T

40312811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52465647-C-T

40312899-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52465562-C-G

40312899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52465562-C-T

40313595-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52464720-T-C

40313839-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52464502-T-A

40313839-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52464502-T-C

http://identifiers.org/hco/13/GRCh38#40313853-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52464488-C-A

http://identifiers.org/hco/13/GRCh38#40313866-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52464485-A-C

40313866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52464485-A-G

40313866-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52464485-A-T

40313924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52464427-C-T

http://identifiers.org/hco/13/GRCh38#40313965-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52464171-A-C

40314028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52464082-C-T

40314227-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52463909-T-C

40314236-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52463897-G-C

40314267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52463872-C-T

http://identifiers.org/hco/13/GRCh38#40315308-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52463029-C-A

40315308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52463029-C-T

40315309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52463028-A-G

http://identifiers.org/hco/13/GRCh38#40315318-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52463022-C-A

40315330-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52463010-G-T

40315353-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52462997-G-T

40315384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52462966-T-C

40315411-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52462800-A-G

40315620-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52462614-G-T

40315624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52462610-T-C

40315694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52462545-C-T

http://identifiers.org/hco/13/GRCh38#40316051-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52462439-A-C

40316119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52462373-G-A

40316275-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52462266-T-G

40316583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52462018-G-A

40316921-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52461799-T-A

40316921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52461799-T-C

40317039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52461694-C-T

40317047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52461686-G-A

40328228-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52456476-T-A

40328461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52456265-A-G

40329006-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52456045-T-C

40329010-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52456040-T-C

40329206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52455853-C-T

40329232-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52455828-T-C

40329486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52455631-C-T

40329569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52455549-C-T

40329609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52455517-G-A

40329675-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52455452-C-G

http://identifiers.org/hco/13/GRCh38#40329697-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52455437-A-C

40333377-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52453814-A-G

40333657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52453559-C-T

40333684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52453528-A-G

40333864-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52453349-T-A

40333958-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52453286-T-C

40333968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52453276-A-G

40334241-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52452825-G-C

40334474-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52452617-A-G

40334499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52452598-C-T

40336082-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52451213-C-G

40336282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52451011-G-A

40336409-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52450906-G-C

40336542-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52450786-T-C

40336835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52450497-G-A

40337798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52449554-G-A

40337804-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52449548-T-C

http://identifiers.org/hco/13/GRCh38#40337979-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52449322-A-C

40338240-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52449106-G-T

40338371-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52448991-G-T

40338591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52448826-G-A

http://identifiers.org/hco/13/GRCh38#40338783-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52448722-C-A

40338892-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52448624-A-G

40339103-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52448424-A-G

40339171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52448379-C-T

40340753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52447593-G-A

40340794-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52447553-T-A

40340805-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52447542-C-G

http://identifiers.org/hco/13/GRCh38#40340996-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52447352-C-A

40341057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52447303-G-A

40341086-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52447272-C-G

40341086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52447272-C-T

40341313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52447065-A-G

40341345-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52447033-T-C

40341417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52446960-C-T

40341975-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52446441-T-C

40342251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52446008-G-A

40342273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52445989-C-T

40342878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52445342-G-A

40342879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52445341-G-A

40342955-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52445279-G-C

40343034-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52445209-T-A

40343424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52444808-C-T

40343434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52444778-A-G

40343473-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52444739-T-A

40343576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52444633-C-T

40343865-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52444342-A-T

http://identifiers.org/hco/13/GRCh38#40344102-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52443801-A-C

40344102-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52443801-A-G

40344111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52443792-C-T

40344183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52443725-G-A

40344183-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52443725-G-T

40344392-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52443527-C-T

40344440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52443475-G-A

40344975-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52442925-G-C

40345363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52442564-G-A

http://identifiers.org/hco/13/GRCh38#40345431-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52442443-A-C

http://identifiers.org/hco/13/GRCh38#40345623-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52442247-C-A

40345777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52442090-G-A

40345793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52442074-G-A

40346232-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52441671-C-G

40346368-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52441563-T-C

http://identifiers.org/hco/13/GRCh38#40346419-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52441510-C-A

40346482-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52441449-C-G

40346572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52441337-C-T

40346899-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52440154-T-C

40347054-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52440014-T-C

40347433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52439675-A-G

http://identifiers.org/hco/13/GRCh38#40347438-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52439670-C-A

40348253-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52439490-A-G

40348338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52439424-G-A

http://identifiers.org/hco/13/GRCh38#40348361-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#52439405-C-A

40348361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 52439405-C-T

40348381-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52439385-G-T

40348432-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 52439334-A-G

40348512-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52439276-G-C

40348512-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52439276-G-T

40348551-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52439237-G-T

40348641-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52439147-G-C

40348641-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52439147-G-T

40348666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52439122-G-A

40348666-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52439122-G-T

40348674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52439114-G-A

40348674-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52439114-G-T

40348711-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52439090-T-A

40348878-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52438952-G-T

40348901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52438929-G-A

40348939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52438906-C-T

40348976-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52438868-T-C

40349114-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52438755-C-G

40349114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52438755-C-T

40349158-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52438714-G-T

40349197-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52438666-G-C

http://identifiers.org/hco/13/GRCh38#40349243-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52438620-C-A

http://identifiers.org/hco/13/GRCh38#40349266-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52438597-C-A

40349266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52438597-C-T

40349292-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52438571-G-T

http://identifiers.org/hco/13/GRCh38#40349351-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52438548-C-A

40349351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52438548-C-T

40349404-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52438498-A-G

40349417-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52438485-A-G

40349444-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52438462-G-C

40349453-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52438453-A-G

40349453-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52438453-A-T

40349457-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52438449-A-G

40349475-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52438430-G-T

http://identifiers.org/hco/13/GRCh38#40349621-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52438283-C-A

40349662-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52438231-G-T

40349673-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52438220-A-G

40349676-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52438213-G-T

40349735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52438153-G-A

40349917-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52437633-T-C

40350021-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52437560-T-C

40350124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: non coding transcript exon variant
orthologous variants: 52437056-A-G

40350179-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: non coding transcript exon variant
orthologous variants: 52437001-T-C

40350179-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: non coding transcript exon variant
orthologous variants: 52437001-T-G

http://identifiers.org/hco/13/GRCh38#40350335-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52436874-A-C

40350371-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52436849-A-G

http://identifiers.org/hco/13/GRCh38#40350406-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52436816-C-A

40350406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52436816-C-T

40350670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52436563-C-T

http://identifiers.org/hco/13/GRCh38#40350767-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52436467-C-A

40350767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52436467-C-T

40351065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52436289-C-T

http://identifiers.org/hco/13/GRCh38#40351389-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52436004-C-A

40351553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52435780-C-T

40351654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52435641-C-T

40351849-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52435428-A-G

http://identifiers.org/hco/13/GRCh38#40352314-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52435201-C-A

40352317-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52435198-T-C

40352615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52434869-C-T

40352731-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52434753-C-T

40352756-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52434714-G-T

40353002-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52434480-T-A

40353045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52434450-G-A

40353093-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52434418-T-C

40353192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52434336-G-A

40353261-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52434269-T-C

40353354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52434215-C-T

40354044-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52433269-T-C

40354049-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52433264-A-G

40354129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52433185-G-A

40354223-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52433102-T-C

40354242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52433083-G-A

http://identifiers.org/hco/13/GRCh38#40354293-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52433044-C-A

40354293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52433044-C-T

40354928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52432857-T-C

40354929-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52432856-T-A

40354951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52432834-G-A

40354951-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52432834-G-T

http://identifiers.org/hco/13/GRCh38#40354968-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52432821-A-C

http://identifiers.org/hco/13/GRCh38#40355275-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52430762-C-A

http://identifiers.org/hco/13/GRCh38#40355335-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52430701-A-C

40355402-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52430634-C-G

40355468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52430580-C-T

40362653-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52429280-C-G

40362653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52429280-C-T

http://identifiers.org/hco/13/GRCh38#40362932-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52429057-C-A

http://identifiers.org/hco/13/GRCh38#40362992-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52429001-C-A

40362992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52429001-C-T

40363081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52428910-G-A

40365797-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52428510-A-T

40365982-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52428336-G-C

40365982-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52428336-G-T

http://identifiers.org/hco/13/GRCh38#40366006-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52428312-C-A

40366006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52428312-C-T

http://identifiers.org/hco/13/GRCh38#40366434-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52427887-C-A

http://identifiers.org/hco/13/GRCh38#40367116-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52427226-A-C

40367177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52427186-G-A

40367182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52427181-C-T

40367770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52426599-G-A

40367940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52426370-C-T

40367972-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52426337-A-G

40367973-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52426336-T-G

40367985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52426324-G-A

40368301-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52425811-A-T

40368465-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52425668-T-A

40368565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52425560-C-T

http://identifiers.org/hco/13/GRCh38#40369356-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52424942-A-C

40369373-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52424925-T-C

40369385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52424913-T-C

40369549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52424751-C-T

40369669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52424666-G-A

40370012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52424333-G-A

40370012-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52424333-G-T

40370182-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52424171-C-G

40370227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52424127-G-A

40370289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52424065-G-A

40370409-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52423949-A-T

40370586-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52423775-A-G

40370586-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52423775-A-T

40375064-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52422704-T-G

40375188-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52422584-A-G

40375381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52422252-G-A

40375386-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52422247-G-C

40375448-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52422183-G-C

40375453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52422178-G-A

40375846-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52421404-G-C

40375863-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52421388-C-G

40376289-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52421080-A-T

40376517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52420878-C-T

40376522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52420873-C-T

40376914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52420605-G-A

40376914-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52420605-G-T

40376960-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52420578-T-A

40376960-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52420578-T-C

40376991-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52420547-A-G

http://identifiers.org/hco/13/GRCh38#40376994-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52420544-C-A

40377013-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52420525-T-C

40377038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52420502-G-A

http://identifiers.org/hco/13/GRCh38#40377058-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52420482-C-A

40377066-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52420474-G-T

http://identifiers.org/hco/13/GRCh38#40377075-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52420469-C-A

40377123-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52420422-G-C

40377123-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52420422-G-T

40379110-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52419115-T-C

40379449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52418798-T-C

40379733-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52418292-C-G

40380611-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52417448-A-T

40380854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52417272-C-T

40380978-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52417149-G-C

40382220-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52416019-A-T

40382226-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52416013-A-G

http://identifiers.org/hco/13/GRCh38#40382256-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52415984-C-A

40382256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52415984-C-T

http://identifiers.org/hco/13/GRCh38#40382455-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52415834-C-A

40382455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52415834-C-T

40382488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52415824-G-A

40382612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52415716-G-A

40383844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52414562-G-A

40383876-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52414535-A-T

40383954-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52414470-T-G

http://identifiers.org/hco/13/GRCh38#40385008-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52413113-A-C

40385056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52413068-T-C

40385639-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52410226-T-A

40385942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52409989-C-T

40386055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52409887-C-T

40386709-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52409125-G-C

40386771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52409066-C-T

40386848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52408999-C-T

http://identifiers.org/hco/13/GRCh38#40388956-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52407453-A-C

40389062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52407371-C-T

40389153-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52407296-G-C

40390449-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52406412-A-G

40390497-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52406364-T-C

http://identifiers.org/hco/13/GRCh38#40390594-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52406268-A-C

40390605-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52406257-C-G

40390752-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52406132-G-T

40390931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52405962-C-T

40390937-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52405956-A-G

40391632-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52404960-G-T

40391639-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52404954-C-G

40391643-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52404950-G-C

40391672-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52404916-G-T

40392294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52404317-G-A

http://identifiers.org/hco/13/GRCh38#40392295-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52404316-C-A

40392305-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52404308-A-G

40392665-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52403979-T-G

40392666-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52403978-A-T

40392735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52403912-C-T

http://identifiers.org/hco/13/GRCh38#40392867-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52403777-A-C

40395074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52400802-G-A

40395129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52400761-T-C

40405353-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52398625-G-C

40405381-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52398597-G-C

40405495-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52398491-A-G

http://identifiers.org/hco/13/GRCh38#40405811-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52398243-A-C

40405811-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52398243-A-G

40405847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52398208-G-A

40406244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52397831-C-T

40406251-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52397824-A-G

http://identifiers.org/hco/13/GRCh38#40406732-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52397515-C-A

40406755-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52397496-A-T

40406761-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52397490-A-T

40406804-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52397449-G-T

40406811-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52397442-A-G

40406919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52397372-T-C

http://identifiers.org/hco/13/GRCh38#40406994-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52397294-C-A

40406994-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52397294-C-G

40407016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52397279-T-C

40407111-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52397100-T-C

40407157-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52397003-T-C

40407318-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52396815-C-G

40407457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52396699-G-A

40407457-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52396699-G-T

40407458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52396698-A-G

40407474-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52396678-A-G

40407475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52396677-C-T

40407660-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52396499-T-C

40408460-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52395861-T-C

40408546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52395775-C-T

40408576-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52395748-T-C

http://identifiers.org/hco/13/GRCh38#40408765-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52395542-A-C

http://identifiers.org/hco/13/GRCh38#40409095-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52395195-A-C

40409493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52394229-C-T

40409494-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52394228-T-G

http://identifiers.org/hco/13/GRCh38#40409692-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52394043-A-C

40409692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52394043-A-G

40409700-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52394035-G-C

40409731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52394004-G-A

40409820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52392712-G-A

40409896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52392644-G-A

40410473-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52392392-G-T

40410760-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52392059-A-G

http://identifiers.org/hco/13/GRCh38#40410763-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52392056-A-C

40410877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52391968-C-T

40411077-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52391794-T-C

40411236-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52391620-T-C

http://identifiers.org/hco/13/GRCh38#40411256-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52391617-C-A

40411256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52391617-C-T

40411332-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52391541-T-C

40411460-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52391420-T-A

40411639-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52391080-A-G

40412476-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52390272-A-G

40412476-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52390272-A-T

40412648-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52389873-T-C

40412781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52389698-C-T

40413007-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52389504-A-G

40413010-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52389501-A-G

40413020-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52389491-C-T

40413032-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52389479-T-C

40413345-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52389215-T-G

40413371-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52389189-A-G

40413384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52389176-T-C

40413688-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52388930-T-C

40413722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52388896-C-T

40413770-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52388862-C-G

40413779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52388853-A-G

40413804-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52388829-A-G

http://identifiers.org/hco/13/GRCh38#40413805-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52388828-C-A

40413824-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52388809-A-G

40415396-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52388248-T-C

40419448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52387267-A-G

40419618-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52387111-A-G

40419790-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52386936-T-C

40420116-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52386614-G-C

40420118-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52386612-T-C

40421049-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52385948-A-T

40421455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52385556-T-C

40421492-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52385519-T-G

40421722-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52385316-A-G

40421722-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52385316-A-T

http://identifiers.org/hco/13/GRCh38#40421723-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52385315-A-C

40421739-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52385303-T-G

http://identifiers.org/hco/13/GRCh38#40421832-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#52385208-C-A

40421851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52385189-G-A

40422466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52384437-C-T

40422577-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52384338-T-A

40422781-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52384140-G-T

40424110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52381463-G-A

40424131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52381442-G-A

40424533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52381081-C-T

40425719-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52380687-T-C

40425720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52380686-G-A

40425720-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52380686-G-C

40425731-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52380675-T-C

40425884-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52380519-C-G

40425977-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52380466-G-T

40426214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52380286-G-A

40426226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52380271-C-T

http://identifiers.org/hco/13/GRCh38#40426268-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52380231-C-A

40426283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52380216-G-A

40426334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52380177-G-A

40427309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52377411-G-A

40427449-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52377265-A-G

40427523-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52377198-T-A

40427803-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52376953-A-G

40427870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52376886-T-C

40428510-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52376027-A-G

40428584-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52375959-G-C

40428592-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52375951-T-A

40428592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52375951-T-C

40428628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52375916-G-A

40428728-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52375827-T-C

40428740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52375815-G-A

40428820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52375737-C-T

40428935-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52375655-A-G

40429006-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52375617-T-C

40429063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52375563-C-T

40429149-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52375478-C-G

40429528-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52375100-A-G

40429604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52374979-A-G

40429743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52374809-T-C

40430531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52374016-G-A

40430672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52373887-C-T

40430708-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52373849-T-A

40430751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52373809-G-A

http://identifiers.org/hco/13/GRCh38#40431376-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52373509-A-C

40431589-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52373318-C-G

http://identifiers.org/hco/13/GRCh38#40431833-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52372604-C-A

40431870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52372551-T-C

http://identifiers.org/hco/13/GRCh38#40431998-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52372440-A-C

40432144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52372303-G-A

40432148-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52372299-A-G

40432268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52372169-G-A

http://identifiers.org/hco/13/GRCh38#40432517-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52371969-C-A

40432517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52371969-C-T

40432714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52371576-G-A

40432838-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52371467-T-C

40432854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52371452-G-A

40432892-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52371418-T-G

40432905-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52371405-T-C

40433096-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52371205-A-G

40433097-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52371204-T-C

40433201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52371123-T-C

40433228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52371100-G-A

http://identifiers.org/hco/13/GRCh38#40433488-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52370994-A-C

40434591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52370484-G-A

40434936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52370196-G-A

40434986-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52370166-T-A

40435297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52369853-C-T

40435298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52369852-G-A

40435315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52369835-G-A

40435326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52369824-G-A

40435448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52369712-C-T

40435647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52369500-C-T

40436009-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52368988-T-C

40436281-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52368833-A-G

40436830-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52368448-A-G

40436836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52368442-G-A

40436846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52368432-A-G

40437316-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52368079-A-G

40437372-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52368024-T-A

40437383-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52368013-T-C

40437383-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52368013-T-G

40437609-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52367709-T-A

http://identifiers.org/hco/13/GRCh38#40437734-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52367585-A-C

40438178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52367219-G-A

40438385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52367141-C-T

40438389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52367138-C-T

http://identifiers.org/hco/13/GRCh38#40438645-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52366860-A-C

40438703-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52366802-T-A

40438703-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52366802-T-C

http://identifiers.org/hco/13/GRCh38#40438704-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52366801-C-A

40438704-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52366801-C-G

40438704-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52366801-C-T

http://identifiers.org/hco/13/GRCh38#40438721-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52366786-C-A

40438721-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52366786-C-G

40438801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52366723-G-A

40438801-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52366723-G-T

40438877-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52366639-T-C

40438924-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52366530-T-C

40439153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52366313-C-T

40439228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52366253-G-A

40439306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52366171-G-A

40440815-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52360754-G-C

40440816-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52360753-C-G

40440826-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52360743-G-T

40441107-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52360505-A-G

http://identifiers.org/hco/13/GRCh38#40441204-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52360392-A-C

40441517-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52359937-C-G

40441891-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52359587-T-C

40442050-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52359458-T-C

40442364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52359165-G-A

40442381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52359148-T-C

40442714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52358987-G-A

40442954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52358792-C-T

40443013-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52358731-T-G

40443409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52358424-G-A

40443443-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52358392-T-G

40443495-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52358340-A-T

40443504-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52358331-T-G

40443638-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52358192-T-G

40444236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52356196-C-T

40444237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52356195-G-A

40444237-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52356195-G-T

40444294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52356141-C-T

40444438-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52356035-T-C

40444574-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52355912-G-A

40444574-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52355912-G-C

40444579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52355907-G-A

40444870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52355637-G-A

40444995-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52355540-T-C

http://identifiers.org/hco/13/GRCh38#40445187-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52355412-A-C

40445461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52355228-G-A

40445469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52355220-G-A

40446548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52350702-C-T

http://identifiers.org/hco/13/GRCh38#40446587-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52350663-A-C

40446587-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52350663-A-G

40446614-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52350636-G-T

40449175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52337001-C-T

40449204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52336972-G-A

40449404-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52336790-G-C

40449857-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52336333-G-C

40449961-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52336230-G-T

40450001-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52336187-G-C

40450427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52335831-C-T

40450436-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52335822-C-G

40450693-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52335489-A-T

40450719-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52335463-G-T

40450783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52335399-C-T

40450888-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52335310-A-G

http://identifiers.org/hco/13/GRCh38#40451008-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52335192-C-A

40451037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52335165-G-A

40451037-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52335165-G-C

40451037-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52335165-G-T

40451099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52335104-G-A

40451130-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52335074-G-T

40451132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52335072-C-T

http://identifiers.org/hco/13/GRCh38#40451241-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52334963-C-A

40451329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52334875-C-T

40451355-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52334848-G-T

40451376-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52334827-T-C

40451377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52334826-C-T

40451421-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52334787-G-C

40451450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52334756-C-T

40456291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52330757-G-A

40456591-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52330492-A-G

40456738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52330358-G-A

40456790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52330327-C-T

40456852-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52330297-C-G

40456981-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52330193-T-C

40457169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52330057-G-A

40457318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52329913-A-G

40457318-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52329913-A-T

http://identifiers.org/hco/13/GRCh38#40457389-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52329816-C-A

40457389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52329816-C-T

40457457-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52329748-A-G

40457553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52329646-G-A

40457553-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52329646-G-T

40457584-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52329615-T-C

40457587-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52329612-T-A

40457587-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52329612-T-C

40457630-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52329574-G-T

40457637-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52329567-C-G

40457637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52329567-C-T

40457639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52329565-C-T

40457758-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52329458-G-T

40458184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52328408-G-A

40458299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52328205-C-T

http://identifiers.org/hco/13/GRCh38#40458329-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52328175-C-A

40458329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52328175-C-T

http://identifiers.org/hco/13/GRCh38#40458361-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52328143-C-A

40458361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52328143-C-T

http://identifiers.org/hco/13/GRCh38#40460347-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52327670-C-A

40464315-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52326533-A-G

40464472-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52326410-C-G

40464473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52326409-G-A

40464747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52326170-C-T

40464844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52326079-C-T

40465057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52325866-C-T

40465082-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52325833-C-G

40465304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52325615-G-A

http://identifiers.org/hco/13/GRCh38#40465818-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52325367-A-C

40465869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52325319-C-T

40466530-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52324519-G-T

40467851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52322769-G-A

40468986-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52321931-G-T

40468991-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52321926-A-G

40469006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52321915-A-G

40469053-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52321873-C-G

40469091-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52321835-T-C

40469213-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52321715-C-G

40469256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52321673-G-A

40469256-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52321673-G-C

40469287-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52321642-G-C

40469372-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52321564-A-G

40469390-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52321545-T-C

http://identifiers.org/hco/13/GRCh38#40469805-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52321334-C-A

40469805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52321334-C-T

40469930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52321210-T-C

40470048-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52321101-T-A

40470048-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52321101-T-C

40470075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52321079-A-G

http://identifiers.org/hco/13/GRCh38#40470312-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52320845-C-A

40470324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52320836-C-T

40470360-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52320806-A-G

http://identifiers.org/hco/13/GRCh38#40470555-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52320663-C-A

40470635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52320582-C-T

http://identifiers.org/hco/13/GRCh38#40470654-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52320563-C-A

40470654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52320563-C-T

40470697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52320543-C-T

40470752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52320487-G-A

40471275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52320046-G-A

http://identifiers.org/hco/13/GRCh38#40472712-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52318184-A-C

http://identifiers.org/hco/13/GRCh38#40472876-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52318051-C-A

http://identifiers.org/hco/13/GRCh38#40473080-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52317869-C-A

40473135-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52317816-T-C

40473160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52317791-A-G

40474302-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52316265-A-G

40474509-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52316074-C-G

40474519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52316064-C-T

40474790-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52315823-T-C

40475033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52315664-C-T

40475130-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52315568-T-C

40475494-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52315390-A-G

40476004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52315057-C-T

http://identifiers.org/hco/13/GRCh38#40476371-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52314771-A-C

40476986-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52314162-T-C

40477047-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52314104-T-C

40477154-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52313986-A-G

40477941-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52312434-T-C

40477941-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52312434-T-G

40478028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52312353-G-A

40478047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52312334-G-A

40478171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52312227-G-A

http://identifiers.org/hco/13/GRCh38#40478382-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52312023-C-A

40478382-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52312023-C-G

http://identifiers.org/hco/13/GRCh38#40478818-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52311007-A-C

40478818-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52311007-A-G

40478859-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52310212-T-C

40478962-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52310043-T-C

http://identifiers.org/hco/13/GRCh38#40479028-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52309988-C-A

40479028-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52309988-C-G

40479262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52309456-G-A

40479278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52309442-T-C

40479328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52309393-C-T

http://identifiers.org/hco/13/GRCh38#40479362-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52309362-C-A

40479448-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52309255-T-C

http://identifiers.org/hco/13/GRCh38#40479753-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52308935-A-C

40479753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52308935-A-G

http://identifiers.org/hco/13/GRCh38#40479865-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52308813-C-A

40479865-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52308813-C-G

40479865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52308813-C-T

40480034-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52308642-G-T

http://identifiers.org/hco/13/GRCh38#40480071-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52308609-C-A

http://identifiers.org/hco/13/GRCh38#40480075-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52308605-C-A

40480075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 52308605-C-T

40480202-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52308477-T-C

40480389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52308326-G-A

40480427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52308294-A-G

40480674-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52307972-G-C

40480854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52307808-T-C

40480920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52307743-G-A

40481006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52307647-G-A

40481060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52307593-C-T

40481119-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52307548-A-G

http://identifiers.org/hco/13/GRCh38#40481202-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52307468-C-A

40481251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52307416-G-A

40481302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52307363-G-A

40481326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52307342-C-T

40481463-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52307201-G-T

40481504-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52307159-A-T

40481995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52306705-A-G

40482168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52306134-G-A

40482224-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52306095-T-G

40482284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52306045-G-A

40482380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52305964-C-T

http://identifiers.org/hco/13/GRCh38#40482390-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52305944-C-A

40484092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52305485-G-A

http://identifiers.org/hco/13/GRCh38#40484625-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52305106-A-C

40484628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52305103-G-A

40484678-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52305069-T-C

40484687-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52305060-G-C

40484696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52305051-G-A

40484914-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52304885-T-G

40484972-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52304824-T-C

40485086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52304711-G-A

40485314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52304511-A-G

40485314-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52304511-A-T

40485518-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52304177-T-A

40485518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52304177-T-C

40485698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52304037-C-T

http://identifiers.org/hco/13/GRCh38#40485929-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#52303805-A-C

40485929-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52303805-A-T

40485959-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52303775-C-G

http://identifiers.org/hco/13/GRCh38#40486408-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52303365-C-A

40486408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52303365-C-T

40486510-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52303260-G-T

40486545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52303225-G-A

40486873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52302588-G-A

http://identifiers.org/hco/13/GRCh38#40486957-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52302522-A-C

40487087-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52302444-T-G

40487230-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52302302-T-A

40487230-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52302302-T-C

40487250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52302282-G-A

40487250-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52302282-G-T

40487276-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52302267-T-G

40487289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52302254-G-A

40487289-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52302254-G-C

40487327-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52302216-G-C

40487353-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52302190-A-G

40489984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52300433-C-T

40490039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52300383-G-A

40490153-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52300222-T-C

40490293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52300105-C-T

40490394-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52300003-T-A

http://identifiers.org/hco/13/GRCh38#40491095-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52299113-C-A

40491359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52298882-G-A

40491361-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52298880-C-G

40491496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52298759-C-T

40491574-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52298683-G-T

40492625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52296154-C-T

40492710-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52296072-A-G

http://identifiers.org/hco/13/GRCh38#40492800-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52296028-C-A

40493041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52295847-C-T

40493100-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52295811-A-G

40493986-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52294836-G-C

40494075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52294745-A-G

40500127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52294035-G-A

40500391-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52293834-C-G

40500391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52293834-C-T

http://identifiers.org/hco/13/GRCh38#40500453-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52293773-A-C

http://identifiers.org/hco/13/GRCh38#40500454-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52293772-A-C

40500501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52293726-T-C

40500501-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52293726-T-G

40500578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52293639-G-A

40500579-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52293638-C-G

http://identifiers.org/hco/13/GRCh38#40500619-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52293598-A-C

40501314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52293200-A-G

http://identifiers.org/hco/13/GRCh38#40501393-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52293120-C-A

40501426-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52293083-T-C

40502547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52292466-G-A

40502547-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52292466-G-T

40503177-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52291980-T-C

40503178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52291979-A-G

40503249-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52291910-T-A

40503249-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52291910-T-C

40503414-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52291774-G-T

40503475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52291707-C-T

40503765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52291433-A-G

40503834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52291365-T-C

40504026-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52291186-T-A

40504321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52290936-C-T

40504521-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52290749-C-G

40505916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52287357-G-A

40506469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52286647-G-A

40506513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52286604-G-A

40506650-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52286493-T-C

40507031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52286096-C-T

40507558-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52285578-T-C

40507571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52285565-G-A

40507582-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52285547-T-G

40507663-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52285429-T-C

40507663-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52285429-T-G

40507664-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52285428-G-T

40507688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52285403-C-T

40507847-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52285218-T-C

40507883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52285189-G-A

40507950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52285154-G-A

40508451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52284625-G-A

40508483-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52284593-T-C

40508653-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52284441-G-A

40508799-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52284308-T-A

40508857-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52284250-C-G

40535261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52277926-A-G

40535339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52277850-G-A

40535339-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52277850-G-T

40535527-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52277675-A-G

http://identifiers.org/hco/13/GRCh38#40535802-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#52277410-C-A

40535802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42770
most severe consequence: non coding transcript exon variant
orthologous variants: 52277410-C-T