85380574-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 75105275-G-A

85380574-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 75105275-G-C

85380620-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 75105324-G-A

http://identifiers.org/hco/15/GRCh38#85380634-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#75105338-C-A

85380634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 75105338-C-T

http://identifiers.org/hco/15/GRCh38#85380652-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#75105356-C-A

85380652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 75105356-C-T

http://identifiers.org/hco/15/GRCh38#85380691-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#75105395-C-A

85380691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 75105395-C-T

85380711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 75105409-G-A

85380711-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 75105409-G-C

85380774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 75105472-G-A

85380774-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 75105472-G-T

85380862-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75105561-A-G

85380863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75105562-G-A

85381005-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75105658-A-T

85381007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75105660-C-T

85381214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75105765-C-T

85381484-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75105984-A-G

85381487-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75105987-T-A

85381768-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 75106202-T-C

85381827-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 75106263-G-T

http://identifiers.org/hco/15/GRCh38#85381910-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75106361-A-C

85381912-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 75106363-A-G

http://identifiers.org/hco/15/GRCh38#85381923-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75106374-C-A

http://identifiers.org/hco/15/GRCh38#85381944-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75106391-A-C

85381944-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 75106391-A-T

http://identifiers.org/hco/15/GRCh38#85382100-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75106508-A-C

85382100-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 75106508-A-G

85382102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 75106510-G-A

http://identifiers.org/hco/15/GRCh38#85382174-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75106587-C-A

85382262-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75106674-A-G

85382746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75107069-G-A

85382901-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75107255-C-G

85383055-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75107444-G-T

85383170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75107539-G-A

85383735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 75108293-G-A

http://identifiers.org/hco/15/GRCh38#85383820-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75108819-C-A

85383820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75108819-C-T

85383892-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75108891-A-G

85383962-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75108945-A-G

85384391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 75109208-G-A

85392937-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75113325-A-G

85392986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75113375-G-A

85393137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75113510-G-A

85393693-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75113945-A-G

85394037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75114219-A-G

85394050-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75114232-A-G

85394410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75114584-C-T

85395097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75115606-C-T

85396627-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75117055-A-G

85396633-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75117061-A-G

85396742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75117170-G-A

http://identifiers.org/hco/15/GRCh38#85396794-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75117204-A-C

85396895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75117297-G-A

85396895-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75117297-G-T

85397239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75117625-A-G

85397299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75117686-C-T

85397465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75117849-G-A

85398005-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75118053-G-C

85398060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75118103-C-T

85398186-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75118189-G-T

85398473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75118471-G-A

85399007-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75118748-T-A

85399020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75118762-G-A

85399057-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75118801-A-G

85399072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75118817-C-T

85406315-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75119614-A-G

85406425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75119702-G-A

85406425-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75119702-G-T

http://identifiers.org/hco/15/GRCh38#85406470-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75119747-A-C

85406631-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75119877-A-T

85406632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75119878-C-T

http://identifiers.org/hco/15/GRCh38#85406690-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75119939-C-A

85406690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75119939-C-T

85407642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75120357-A-G

85407686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75120397-G-A

85407773-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75120500-G-T

85407944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75120656-G-A

85407980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75120687-G-A

85408085-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75120790-G-C

85408312-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75121075-C-G

85408341-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75121099-C-T

85408342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75121100-G-A

85408446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75121197-C-T

85408835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75121524-T-C

85414050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75122139-G-A

http://identifiers.org/hco/15/GRCh38#85414266-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75122343-C-A

85414360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75122439-T-C

85414414-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75122495-T-G

85415969-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75123702-G-T

85416493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75124497-C-T

85419178-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75126124-A-T

85419372-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75126498-A-G

85420450-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75126874-A-G

85420674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75127254-C-T

http://identifiers.org/hco/15/GRCh38#85420776-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75127355-A-C

85420776-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75127355-A-G

85420834-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75127408-G-T

85420985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75127461-G-A

85421289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75128016-G-A

85421308-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75128035-C-G

85421308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75128035-C-T

85421324-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75128051-A-T

85425762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75130109-C-T

85426052-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75130385-A-G

85427996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75133730-C-T

85428027-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75133745-C-G

85428067-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75133768-G-T

85428140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75133836-C-T

85428597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75134014-A-G

85428721-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75134101-A-G

85429583-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75135841-T-C

85429881-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75136130-A-T

http://identifiers.org/hco/15/GRCh38#85429955-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75138283-C-A

85430033-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75138352-G-T

85430599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75138904-C-T

85430711-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75139022-A-G

http://identifiers.org/hco/15/GRCh38#85430919-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75139212-C-A

85431326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75140403-T-C

85431684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75140803-G-A

85431684-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75140803-G-T

85431925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75141008-G-A

85432070-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75141269-A-G

http://identifiers.org/hco/15/GRCh38#85432236-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75141433-C-A

85433530-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75143028-A-G

85433562-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75143059-T-C

85433694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75143183-C-T

85433740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75143236-G-A

85433740-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75143236-G-C

85433740-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75143236-G-T

85440091-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75143342-T-C

85440125-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75143376-A-G

85440131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75143382-G-A

85440685-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75144282-C-G

85440692-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75144289-T-A

85440694-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75144291-T-C

85441017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75144596-G-A

85441271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75144798-C-T

85441332-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75144850-A-G

85441356-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75144946-A-G

85441432-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75145188-C-G

85441554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75145328-G-A

http://identifiers.org/hco/15/GRCh38#85441592-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75145348-C-A

85441592-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75145348-C-G

85441738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75145548-G-A

85441785-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75145682-A-T

85441922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75145904-C-T

85442687-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75146215-A-G

85442848-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75146463-A-G

85443208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75146780-C-T

85443281-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75146853-T-G

85444048-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, undefined
orthologous variants: 75148609-A-G

85444063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75148624-G-A

85444117-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, undefined
orthologous variants: 75148678-C-G

85444258-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75148814-A-G

85444645-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75149140-A-T

85444876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75149332-G-A

http://identifiers.org/hco/15/GRCh38#85444955-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75149393-A-C

85445059-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75149480-T-C

85445543-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75149926-T-C

85445627-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75150009-C-G

85445747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75150074-A-G

85446163-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75150251-A-G

http://identifiers.org/hco/15/GRCh38#85455375-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75155304-A-C

85456805-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75155676-A-G

85456860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75155731-G-A

85456913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75155772-G-A

85456913-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75155772-G-T

85457023-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75155873-T-C

85457026-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75155876-A-G

85457204-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75156017-A-G

85457219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75156032-G-A

85457256-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75156070-G-C

85457256-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75156070-G-T

85457518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75156509-T-C

85457518-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75156509-T-G

85457805-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75156822-C-G

85457805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75156822-C-T

http://identifiers.org/hco/15/GRCh38#85458223-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75157170-C-A

85458266-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75157222-T-C

http://identifiers.org/hco/15/GRCh38#85458369-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75157312-C-A

85458369-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75157312-C-G

85458369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75157312-C-T

85458418-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75157323-G-T

85458650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75157555-G-A

85458650-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75157555-G-C

85458650-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75157555-G-T

85459025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75158152-G-A

85459094-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, undefined
orthologous variants: 75158218-G-A

85459207-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, undefined
orthologous variants: 75158327-C-G

85460050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75158559-G-A

http://identifiers.org/hco/15/GRCh38#85460151-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75158665-A-C

http://identifiers.org/hco/15/GRCh38#85460156-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75158675-A-C

85460156-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75158675-A-G

85460254-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75158761-T-C

85460802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75159256-C-T

85460860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75159327-C-T

85461001-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75159460-A-G

85461606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75159847-G-A

85461606-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75159847-G-T

85461759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75160017-G-A

85461947-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75160190-G-C

85463240-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75165055-A-G

http://identifiers.org/hco/15/GRCh38#85463325-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75165124-C-A

85463325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75165124-C-T

85463362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75165160-C-T

85463452-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75165257-C-G

85463452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75165257-C-T

85463637-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75165348-T-A

85463656-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75165365-C-G

85463846-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75165475-G-T

85463880-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75165509-A-G

85464170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75165785-C-T

http://identifiers.org/hco/15/GRCh38#85464300-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75165888-A-C

85464357-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75165919-T-C

85464364-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75165926-T-A

85474481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75173906-A-G

85475049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75174756-G-A

85475121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75174822-G-A

85476369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75176586-C-T

85476510-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75176721-A-G

85477038-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75176985-A-G

85477517-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75177451-T-C

85477991-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, undefined
orthologous variants: 75177873-G-C

85477991-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, undefined
orthologous variants: 75177873-G-T

85478050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75177932-C-T

85478084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75177964-G-A

85478338-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75178211-C-T

85478417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75178321-C-T

85478598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75178482-C-T

http://identifiers.org/hco/15/GRCh38#85478626-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75178511-C-A

85478936-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75178817-A-G

85479053-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75178936-A-T

85479166-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75179027-T-C

85479298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75179144-G-A

http://identifiers.org/hco/15/GRCh38#85479375-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75179226-C-A

85479555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75179387-G-A

85480576-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75180528-A-G

85480791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75180685-G-A

85480791-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75180685-G-T

85480810-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75180700-C-G

85480810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75180700-C-T

http://identifiers.org/hco/15/GRCh38#85480842-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75180730-C-A

85480842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75180730-C-T

85481352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75181190-T-C

85481789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75181519-G-A

85481802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75181525-G-A

85481904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75181618-G-A

85482870-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75181929-G-T

85483040-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75182098-A-T

85484051-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75182373-A-G

http://identifiers.org/hco/15/GRCh38#85484110-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75182432-A-C

85484272-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75182684-T-C

85484272-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75182684-T-G

85484390-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75182892-T-C

85484446-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75182947-G-C

85484526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75183013-G-A

85484609-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75183063-T-C

85484618-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75183070-G-T

85484670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75183218-G-A

85484703-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75183266-G-C

85484703-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75183266-G-T

85484822-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75183383-C-G

85484957-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75183506-T-C

85484958-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75183507-C-G

85485167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75184019-A-G

85485167-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75184019-A-T

85485272-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75184136-A-G

85485491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75184298-A-G

85485570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75184383-G-A

85485570-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75184383-G-T

85485580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75184393-G-A

85485580-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75184393-G-T

http://identifiers.org/hco/15/GRCh38#85485586-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75184400-A-C

85485586-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75184400-A-G

85485586-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75184400-A-T

http://identifiers.org/hco/15/GRCh38#85485602-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75184421-C-A

85485602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75184421-C-T

http://identifiers.org/hco/15/GRCh38#85485606-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75184439-A-C

http://identifiers.org/hco/15/GRCh38#85485616-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75184449-C-A

85485616-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75184449-C-T

http://identifiers.org/hco/15/GRCh38#85485626-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75184459-C-A

85485738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: synonymous variant
orthologous variants: 75184584-G-A

85485738-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: missense variant
orthologous variants: 75184584-G-T

85485802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75184639-T-C

http://identifiers.org/hco/15/GRCh38#85485859-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75184692-C-A

85485859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75184692-C-T

85485864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75184697-G-A

85485864-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75184697-G-T

http://identifiers.org/hco/15/GRCh38#85485890-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75184718-C-A

85485918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, undefined
orthologous variants: 75184746-T-C

85486142-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, undefined
orthologous variants: 75184967-T-A

85489343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75186537-C-T

85489708-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75186847-A-G

85489791-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, undefined
orthologous variants: 75186931-G-T

85489848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75187100-C-T

85489940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75187190-G-A

85489998-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75187245-A-G

85490019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75187266-G-A

85490084-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, undefined
orthologous variants: 75187320-T-C

85490498-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75187675-G-C

85490879-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75188277-T-C

85490938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75188335-G-A

85490938-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75188335-G-C

85491051-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75188427-G-T

85491122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75188499-G-A

85491211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75188582-C-T

http://identifiers.org/hco/15/GRCh38#85491212-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75188583-A-C

85491212-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75188583-A-G

85491862-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75189711-C-G

85491963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75189764-A-G

85492071-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75189833-A-T

85492218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75189950-A-G

85492535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75190061-A-G

85492547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75190073-C-T

85492548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75190074-C-T

85493064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75190771-G-A

85493064-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75190771-G-T

85494227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75198761-G-A

85494310-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, undefined
orthologous variants: 75198834-T-G

85494692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, undefined
orthologous variants: 75199159-G-A

85494965-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75199421-T-C

85495186-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75199616-A-G

85495230-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75199657-A-G

85495279-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75199705-A-G

85495478-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75199899-A-T

http://identifiers.org/hco/15/GRCh38#85495521-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75199959-A-C

http://identifiers.org/hco/15/GRCh38#85495555-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75199992-C-A

85495555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75199992-C-T

http://identifiers.org/hco/15/GRCh38#85495609-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75200036-A-C

85495835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75200259-T-C

85496020-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75200480-C-T

85496244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75200673-C-T

85496508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75200947-C-T

85496601-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75201029-A-G

85496690-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75201118-A-T

85497043-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75201438-T-C

85497163-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75201558-A-G

85497369-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75201716-A-G

85499494-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75202578-T-G

85499767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75202822-A-G

http://identifiers.org/hco/15/GRCh38#85501115-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75204228-C-A

85501115-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75204228-C-G

85501131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75204244-C-T

85501242-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75204347-G-T

85501611-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75204731-A-G

85501611-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75204731-A-T

85504808-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75205334-A-T

85504847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75205372-C-T

85505249-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75205857-T-C

http://identifiers.org/hco/15/GRCh38#85505289-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75205896-A-C

85505393-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75205995-A-G

85505456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75206053-C-T

85505749-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75206298-T-C

85505830-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75206363-T-C

85506339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75206553-G-A

85506400-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75206600-T-G

85506769-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75206839-A-G

85506873-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75206935-A-G

85506910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75206972-G-A

http://identifiers.org/hco/15/GRCh38#85506991-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75207049-A-C

85507079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75207142-C-T

85507921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75208281-C-T

85507924-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75208284-G-A

http://identifiers.org/hco/15/GRCh38#85509904-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75209378-C-A

85510244-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75209901-G-C

85514482-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75212108-T-C

85514565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75212189-A-G

85514813-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75212414-A-G

85515007-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75212579-G-T

85515515-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75213006-A-G

85516965-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75216515-T-G

85517273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75216793-C-T

85517315-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75216828-C-G

85517510-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75217006-G-T

85517895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75217351-T-C

85517957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75217408-G-A

85517957-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75217408-G-T

85518013-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75217464-A-T

85518104-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75217549-A-T

85518178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75217616-G-A

85518293-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75217737-G-C

85518293-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75217737-G-T

85518298-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75217741-A-G

85518298-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75217741-A-T

85518451-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75217875-T-C

85518986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75218029-G-A

85519424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75218287-A-G

85519794-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75218755-T-C

85519886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75218840-C-T

85519888-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75218842-C-G

85520077-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75219050-A-T

85520086-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75219059-A-G

85520107-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75219077-A-T

http://identifiers.org/hco/15/GRCh38#85520562-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75219220-C-A

85520562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75219220-C-T

85520708-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75219365-A-G

85520918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75219500-C-T

85520966-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75219561-T-G

85520974-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75219569-T-C

85520978-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75219573-G-T

85521556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: synonymous variant
orthologous variants: 75219760-A-G

85521614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75219818-T-C

85522999-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75221273-C-G

85523072-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75221327-G-T

85523222-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75221441-A-G

85523404-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75221637-G-T

85523638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75221836-G-A

85523670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75221862-C-T

85523750-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75221929-A-T

85524735-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75222572-A-G

http://identifiers.org/hco/15/GRCh38#85524791-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75222608-C-A

85524791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75222608-C-T

http://identifiers.org/hco/15/GRCh38#85524865-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75222694-C-A

85525501-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75223134-A-T

85525875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75223466-G-A

85525987-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75223577-G-T

85526049-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75223643-T-A

85526049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75223643-T-C

85526077-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75223671-A-G

85526907-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75224365-A-G

85527310-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75224450-A-G

85527443-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75224598-A-G

85527668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75224838-C-T

http://identifiers.org/hco/15/GRCh38#85527701-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75224871-C-A

http://identifiers.org/hco/15/GRCh38#85527914-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75225064-C-A

http://identifiers.org/hco/15/GRCh38#85528211-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75225383-A-C

85528445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75225635-G-A

85528537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75225720-G-A

85528591-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75225768-A-G

http://identifiers.org/hco/15/GRCh38#85528645-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75225822-A-C

85529085-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75226192-G-C

85532692-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75228447-G-T

85532716-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75228472-A-G

85532729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75228485-G-A

http://identifiers.org/hco/15/GRCh38#85532846-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75228592-A-C

85532846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75228592-A-G

85532866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75228612-C-T

85533108-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75228831-A-T

85533202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75228899-C-T

85533277-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75228975-T-G

85533458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75229137-A-G

85533494-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75229167-G-T

http://identifiers.org/hco/15/GRCh38#85533521-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75229194-A-C

85533521-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75229194-A-T

85533642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: synonymous variant
orthologous variants: 75229308-C-T

85533879-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 75229545-T-C

85533904-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, missense_variant
orthologous variants: 75229569-A-G

85533923-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, missense_variant
orthologous variants: 75229581-T-C

http://identifiers.org/hco/15/GRCh38#85533972-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75229617-C-A

85534025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 75229655-T-C

http://identifiers.org/hco/15/GRCh38#85534026-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75229656-C-A

85534026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 75229656-C-T

85534231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 75229798-G-A

85534231-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 75229798-G-T

85534251-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 75229820-A-G

85534251-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 75229820-A-T

85534303-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 75229871-G-A

85534303-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 75229871-G-T

85534308-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 75229876-A-G

http://identifiers.org/hco/15/GRCh38#85534343-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75229910-C-A

85534343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 75229910-C-T

85538019-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75231094-G-C

85538039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75231114-G-A

http://identifiers.org/hco/15/GRCh38#85538047-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75231122-A-C

85538047-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75231122-A-T

85538142-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75231248-T-G

85538339-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75231403-G-C

http://identifiers.org/hco/15/GRCh38#85538457-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75231511-A-C

85538457-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75231511-A-T

85539183-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75231621-T-G

85539415-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75231878-G-T

85539497-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75231956-G-T

85539553-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75232017-C-G

85540285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75232486-G-A

85540420-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75232629-T-C

85540534-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75232741-G-C

85540847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75233254-G-A

85541122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75233516-A-G

85541329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75233767-C-T

85541393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75233834-G-A

http://identifiers.org/hco/15/GRCh38#85541929-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75233922-A-C

85541930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75233923-G-A

85542181-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75234194-C-G

85542181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75234194-C-T

85543106-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75235228-T-C

85543431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75235522-G-A

85543431-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75235522-G-T

85543663-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75235779-A-G

85543669-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, undefined
orthologous variants: 75235785-A-T

85543719-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75235849-T-C

85543719-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75235849-T-G

85543739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, undefined
orthologous variants: 75235869-C-T

85543764-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, splice_region_variant, undefined
orthologous variants: 75235897-A-G

85543815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: synonymous variant
orthologous variants: 75235948-G-A

http://identifiers.org/hco/15/GRCh38#85543885-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: missense_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#75236018-C-A

85543885-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: missense_variant, undefined
orthologous variants: 75236018-C-G

85543975-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75236104-T-C

85543990-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75236119-A-G

85543994-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75236123-C-G

85544081-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 75236168-T-G

85544091-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 75236180-T-A

85544091-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 75236180-T-C

85544091-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 75236180-T-G

85544092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 75236181-G-A

85544092-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 75236181-G-T

85544101-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 75236190-T-C

85544126-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 75236215-A-G

85544126-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 75236215-A-T

85544152-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75236239-T-A

85544257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75236330-A-G

85544260-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75236333-A-G

85544319-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75236393-A-G

85544876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75236893-C-T

85544934-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75236954-T-A

85544934-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75236954-T-C

85544937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75236957-G-A

85545070-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75237117-A-G

85545102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75237151-G-A

http://identifiers.org/hco/15/GRCh38#85545199-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75237243-A-C

85545199-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75237243-A-G

85545375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75237432-G-A

85545530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75237561-C-T

85545566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75237595-G-A

85545662-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75237689-C-G

85547571-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75240702-G-T

85547578-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75240709-A-G

85547787-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75240833-T-C

85547935-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75240946-T-C

http://identifiers.org/hco/15/GRCh38#85548049-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75241055-A-C

85548122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75241108-G-A

85548399-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75241367-A-G

85548422-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75241390-G-T

85548427-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75241395-T-G

85548428-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75241396-A-G

http://identifiers.org/hco/15/GRCh38#85548469-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75241425-A-C

85548469-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75241425-A-T

85548487-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75241443-A-G

85548598-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75241544-A-G

85549869-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75242326-G-A

85549885-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75242342-G-C

85550430-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75242597-G-T

85550661-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75242788-C-G

85550671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75242798-G-A

85550711-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75242838-C-G

85550711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75242838-C-T

85550853-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75242966-G-A

85550853-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75242966-G-T

85550967-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75243077-A-G

85550967-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75243077-A-T

85552171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: -G-A

85552171-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: -G-T

85552248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: -A-G

85552431-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: -A-G

85552431-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: -A-T

85552549-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: -G-T

85553665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: -A-G

85555243-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75245953-G-T

85555244-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75245954-T-C

85555244-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75245954-T-G

85555267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75245977-A-G

85555287-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75245997-T-A

85555287-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75245997-T-C

85555287-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75245997-T-G

85555319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75246030-G-A

85555319-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75246030-G-T

85555326-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75246037-G-T

85555329-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75246040-A-G

85555346-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75246057-A-G

85555379-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75246090-A-G

85555401-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75246113-G-C

85555432-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75246144-A-G

85555621-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75246323-A-G

85555715-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75246417-G-T

http://identifiers.org/hco/15/GRCh38#85555716-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75246418-C-A

85555716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75246418-C-T

85555978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75246698-T-C

85555978-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75246698-T-G

85557356-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75247438-T-C

85557420-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75247501-A-G

85558140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75247788-G-A

85558164-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75247807-T-C

85558496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75248105-G-A

85558496-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75248105-G-C

85564661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75250091-C-T

85564803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75250203-C-T

85565138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75250491-G-A

85565138-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75250491-G-T

85565168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75250518-G-A

85565218-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75250566-G-T

85565231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75250579-C-T

http://identifiers.org/hco/15/GRCh38#85565473-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75250816-A-C

http://identifiers.org/hco/15/GRCh38#85565525-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75250850-A-C

http://identifiers.org/hco/15/GRCh38#85565600-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75250924-A-C

85565701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75251031-A-G

85573969-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75251147-T-C

85574179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75251354-G-A

85574179-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75251354-G-T

85574206-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75251379-A-G

85574722-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75252128-A-G

85574778-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75252183-G-T

85574812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75252221-C-T

85574858-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75252264-A-G

85574981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75252392-G-A

85574981-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75252392-G-T

85575246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 75252649-G-A

85575399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75252768-G-A

85575399-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75252768-G-T

85576139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75254940-G-A

85576157-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75254964-G-C

85576326-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75255133-T-G

85576327-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75255134-A-G

85576671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75255443-C-T

85578829-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75258098-G-T

85579138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75258447-C-T

85579207-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 75258513-G-C

85579216-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75258522-T-C

85579244-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 75258550-A-T

85579270-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75258576-T-C

85579290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75258596-G-A

85579290-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 75258596-G-T

http://identifiers.org/hco/15/GRCh38#85579310-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75258616-C-A

85579310-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 75258616-C-G

85579569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75258875-G-A

85579569-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75258875-G-C

85579571-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 75258877-G-T

85579606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75258912-T-C

85579606-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75258912-T-G

85579677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75258983-G-A

85579716-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75259022-G-C

85579875-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 75259178-C-G

85579875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 75259178-C-T

85580007-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 75259307-G-T

http://identifiers.org/hco/15/GRCh38#85580039-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75259336-A-C

85580039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 75259336-A-G

85580149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 75259443-C-T

85580186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: synonymous_variant, undefined
orthologous variants: 75259477-C-T

85580219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: synonymous_variant, undefined
orthologous variants: 75259510-C-T

85580263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: missense_variant, undefined
orthologous variants: 75259554-G-A

85580367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: missense variant
orthologous variants: 75259658-C-T

85580616-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: missense variant
orthologous variants: 75259904-T-A

85580651-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: synonymous variant
orthologous variants: 75259936-G-T

85580694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: missense variant
orthologous variants: 75259979-G-A

85580694-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: missense variant
orthologous variants: 75259979-G-C

85580694-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: missense variant
orthologous variants: 75259979-G-T

http://identifiers.org/hco/15/GRCh38#85580696-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75259981-C-A

http://identifiers.org/hco/15/GRCh38#85580700-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75259985-C-A

85580700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: missense variant
orthologous variants: 75259985-C-T

http://identifiers.org/hco/15/GRCh38#85580701-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75259986-C-A

85580701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: missense variant
orthologous variants: 75259986-C-T

85580716-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: missense variant
orthologous variants: 75260001-C-G

85580787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: missense variant
orthologous variants: 75260057-G-A

85580818-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: missense variant
orthologous variants: 75260088-T-A

85581313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: missense variant
orthologous variants: 75260562-A-G

85581417-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: missense variant
orthologous variants: 75260666-A-G

85581417-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: missense variant
orthologous variants: 75260666-A-T

85581436-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: missense variant
orthologous variants: 75260682-G-T

85581476-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: synonymous variant
orthologous variants: 75260722-A-G

85581626-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: synonymous variant
orthologous variants: 75260857-C-G

85581626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: synonymous variant
orthologous variants: 75260857-C-T

85581732-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: missense variant
orthologous variants: 75260965-G-C

85581842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: synonymous variant
orthologous variants: 75261064-T-C

85581870-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: missense variant
orthologous variants: 75261092-G-C

85581969-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: missense variant
orthologous variants: 75261179-A-G

85581969-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: missense variant
orthologous variants: 75261179-A-T

http://identifiers.org/hco/15/GRCh38#85582098-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75261287-C-A

85582098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: missense variant
orthologous variants: 75261287-C-T

85582136-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75261326-G-T

85582190-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75261364-G-C

85582190-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75261364-G-T

http://identifiers.org/hco/15/GRCh38#85582265-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75261439-A-C

85582265-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75261439-A-G

85582483-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75261637-G-T

85582569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75261718-C-T

85582765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75261873-G-A

85582765-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75261873-G-T

85582804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75261911-G-A

85582804-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75261911-G-T

http://identifiers.org/hco/15/GRCh38#85582826-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75261933-C-A

85582826-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75261933-C-G

85582826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75261933-C-T

85582837-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75261944-T-G

85582916-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 75262024-A-G

85582959-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 75262068-A-G

85582960-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 75262069-A-G

85583042-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 75262149-G-C

85583179-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75262263-G-T

85583226-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75262300-A-G

85583269-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75262353-G-T

85583343-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75262423-T-C

85583535-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75262599-C-G

85583535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75262599-C-T

85583565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75262629-G-A

http://identifiers.org/hco/15/GRCh38#85583787-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75262885-C-A

85583787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75262885-C-T

85583904-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75262988-A-G

85583973-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, undefined
orthologous variants: 75263044-T-C

85583983-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75263047-C-G

http://identifiers.org/hco/15/GRCh38#85583984-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75263048-A-C

85583984-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75263048-A-G

85584009-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, undefined
orthologous variants: 75263072-T-G

85584340-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, undefined
orthologous variants: 75263374-T-G

85584570-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75263569-G-C

85584717-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75263715-C-G

85585015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75263973-C-T

85585561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75264533-G-A

85585561-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75264533-G-T

85585595-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75264547-A-T

85585603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75264555-G-A

85585623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75264574-C-T

85585638-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75264589-A-G

85585652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75264603-A-G

85585679-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75264647-C-G

85585690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75264658-C-T

85585843-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75264816-C-G

85585843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75264816-C-T

85586056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75265007-T-C

85586148-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75265097-A-T

http://identifiers.org/hco/15/GRCh38#85588005-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75266089-C-A

85588100-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75266166-A-G

85588186-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75266253-C-G

85588455-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75266528-A-T

85588542-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75266548-C-G

85590237-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, undefined
orthologous variants: 75268773-A-T

85590401-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75268895-G-C

85590446-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75268943-C-G

85590446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75268943-C-T

85590553-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75269106-T-C

85590776-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75269495-T-C

85590814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75269512-G-A

85590814-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75269512-G-C

85590866-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75269540-G-C

http://identifiers.org/hco/15/GRCh38#85590869-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75269541-C-A

85590875-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75269547-A-G

85590888-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75269563-A-G

85590969-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75269636-T-A

85591191-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75269834-T-C

85591326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75269959-C-T

85591721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75270369-G-A

85591971-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75270619-G-T

85592068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75270702-G-A

85592068-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75270702-G-T

85592357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, undefined
orthologous variants: 75270974-G-A

85592579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75271191-C-T

85592614-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75271228-C-G

http://identifiers.org/hco/15/GRCh38#85592629-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75271243-C-A

85592704-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75271305-G-C

85592784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75271386-G-A

85592784-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75271386-G-C

85592876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75271478-G-A

85593623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75271788-G-A

85593626-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75271791-T-C

85593629-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75271794-T-C

85593764-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75271975-A-T

85593933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75272071-G-A

85594095-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75272220-A-G

85594182-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75272304-T-G

85594257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75272372-A-G

85594297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75272412-G-A

85594517-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75272601-A-G

85594517-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75272601-A-T

85594583-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75272667-T-C

85594614-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75272688-C-G

85594623-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75272697-C-G

85594690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75272765-A-G

85594754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75272830-C-T

85594834-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75272901-G-A

http://identifiers.org/hco/15/GRCh38#85594864-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75272932-C-A

85594864-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75272932-C-G

85594864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75272932-C-T

85594971-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75273000-T-C

85595567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75273215-G-A

85595589-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75273220-T-C

85595691-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75273312-A-G

85595905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75273492-A-G

85596097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75273666-A-G

85596754-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75274334-A-G

85596932-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75274542-A-G

85596968-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75274588-T-C

85596968-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75274588-T-G

85597059-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75274809-A-T

85597187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75274930-G-A

85597232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75274965-C-T

85597248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75274981-A-G

85597264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75274995-C-T

85597345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75275057-C-T

85597699-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75275452-G-C

85598309-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75276705-G-T

http://identifiers.org/hco/15/GRCh38#85598341-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75276736-C-A

85598402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75276787-C-T

85598560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75276947-C-T

http://identifiers.org/hco/15/GRCh38#85598662-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75277043-A-C

85598800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75277150-G-A

85598800-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75277150-G-C

85598881-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75277222-A-G

85599959-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75277933-C-G

85600338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75278236-G-A

85600508-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75278378-T-A

85600604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75278460-C-T

85600611-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75278467-G-T

85600728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75278704-G-A

85600728-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75278704-G-C

85600909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75278873-C-T

85601030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75278973-C-T

85607354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75281840-T-C

85607376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75281861-A-G

85607582-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75282107-C-G

85607582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75282107-C-T

85607664-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75282174-A-G

85607789-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75282478-C-G

85607789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75282478-C-T

85607947-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75283923-G-T

85608007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, undefined
orthologous variants: 75284008-G-A

85608074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, undefined
orthologous variants: 75284071-G-A

85608116-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75284113-G-T

85608309-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75284557-C-G

85608542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75284797-G-A

85608690-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75284944-T-C

85612899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75287651-G-A

85615091-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75288507-T-C

85615101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75288517-A-G

85615179-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75288592-G-C

85615248-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75288666-G-T

85615261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75288679-G-A

85615261-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75288679-G-C

85615268-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75288686-A-G

85615675-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75289005-T-C

85615931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75289260-C-T

85615998-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75289330-T-G

85616120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75289433-C-T

85616571-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75289804-G-C

85616681-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75289912-G-C

85616694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75289925-A-G

85616831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75290061-G-A

85616991-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75290232-A-T

85616992-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75290233-A-G

http://identifiers.org/hco/15/GRCh38#85617074-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75290313-A-C

85617851-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75290750-C-G

85618116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75290979-G-A

http://identifiers.org/hco/15/GRCh38#85618117-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75290980-C-A

85618315-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75291189-A-G

85618315-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75291189-A-T

85618479-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75291546-T-G

85618579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75291642-G-A

85618962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75291986-G-A

85619298-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, undefined
orthologous variants: 75292330-G-C

85619298-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, undefined
orthologous variants: 75292330-G-T

85619321-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75292353-A-G

85619515-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75292577-T-A

http://identifiers.org/hco/15/GRCh38#85619590-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75292641-A-C

85619590-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75292641-A-G

85619590-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75292641-A-T

85619614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75292663-G-A

85619614-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75292663-G-T

85619716-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 75292764-A-T

http://identifiers.org/hco/15/GRCh38#85619721-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75292769-A-C

85619721-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 75292769-A-G

85619721-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 75292769-A-T

http://identifiers.org/hco/15/GRCh38#85619771-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75292819-C-A

85619771-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 75292819-C-G

85619771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 75292819-C-T

85619823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 75292866-G-A

85620201-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75293242-G-C

85620243-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75293282-T-C

85620300-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75293354-T-A

85620316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75293375-G-A

85620316-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75293375-G-T

85620350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75293448-G-A

85620354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75293452-C-T

85620604-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75293702-C-G

85620751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75293810-G-A

85620751-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75293810-G-C

85620791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75293855-C-T

85620828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75293891-C-T

http://identifiers.org/hco/15/GRCh38#85620982-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75294045-A-C

85621055-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75294124-G-T

http://identifiers.org/hco/15/GRCh38#85621155-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75294230-C-A

85621159-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75294243-T-C

85621297-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75294639-A-G

85621364-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75294696-A-T

85622604-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75296379-A-T

85622621-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75296396-T-C

85622780-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75296552-A-G

85623335-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75297628-A-T

http://identifiers.org/hco/15/GRCh38#85623440-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75297736-C-A

85623514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75297810-C-T

85623553-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75297843-T-G

85623741-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75298048-A-G

85623793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75298107-G-A

85623839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75298159-G-A

85624146-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75298470-T-C

85624171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75298494-G-A

85624369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75298686-G-A

85624369-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75298686-G-T

http://identifiers.org/hco/15/GRCh38#85624388-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75298705-C-A

85624608-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75298731-G-T

85624641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75298764-A-G

85624741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75298863-G-A

85624741-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75298863-G-C

85624741-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75298863-G-T

85624916-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75299019-C-G

85624985-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75299087-T-C

85624996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75299098-C-T

85625769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75299659-G-A

85625794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75299683-G-A

85626285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75300162-G-A

85626396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75300267-C-T

85626439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75300302-G-A

http://identifiers.org/hco/15/GRCh38#85626544-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75300390-A-C

85626756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75300581-C-T

85627199-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75300917-T-A

85627199-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75300917-T-C

85631903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75303277-G-A

85631916-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75303290-A-G

85631990-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75303367-A-G

85632114-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75303485-G-C

85633549-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75304208-T-C

85639264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75313063-G-A

85639264-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75313063-G-T

85639358-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75313144-T-C

85639448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, synonymous_variant
orthologous variants: 75313234-A-G

85639464-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75313241-T-C

http://identifiers.org/hco/15/GRCh38#85639525-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75313291-C-A

85639525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75313291-C-T

85639575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75313341-G-A

85639575-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75313341-G-T

85639592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75313358-G-A

85639592-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75313358-G-T

85639600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75313366-G-A

85639871-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75314139-G-C

85639946-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75314185-A-G

85640130-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75314328-T-C

85640212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75314402-C-T

85640307-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75314512-G-C

85640699-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75314700-G-T

85640700-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75314701-T-G

85640767-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75314759-T-C

85640850-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75314830-T-G

85640924-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75314902-A-G

85642707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75315484-G-A

85642734-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75315511-A-G

85642996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75315759-G-A

85643179-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75315918-C-G

85645672-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75316143-A-G

85645672-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75316143-A-T

85645787-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75316218-T-C

85645787-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75316218-T-G

85645949-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 75316391-C-G

http://identifiers.org/hco/15/GRCh38#85645977-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75316419-A-C

85645977-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75316419-A-G

http://identifiers.org/hco/15/GRCh38#85646697-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#75316970-A-C

85646903-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75317105-C-G

85648016-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75317642-T-A

85649101-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75318485-A-T

85649229-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75319107-A-G

85649436-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75319285-A-G

85649460-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75319303-A-T

85649505-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75319359-A-T

85649665-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75319474-T-C

85650916-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75319717-T-A

85650994-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75319784-A-G

85651328-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75320097-A-T

85651351-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75320107-G-C

85651416-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75320181-A-G

85651433-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75320197-T-C

85652060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75323146-C-T

85653176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75324150-A-G

85653242-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75324213-A-G

http://identifiers.org/hco/15/GRCh38#85653297-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75324267-C-A

85653352-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75324321-G-T

85653404-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75324372-G-C

85653412-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75324380-T-G

85653518-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75324466-C-G

85653575-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75324530-A-G

85653679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75324632-T-C

85653731-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75324707-T-C

85653738-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75324714-G-T

85654129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75325199-T-C

85654302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75325332-G-A

85655351-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75326783-A-G

85655356-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75326788-A-G

85655504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 75326941-G-A

85655504-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 75326941-G-T

http://identifiers.org/hco/15/GRCh38#85655588-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75327025-A-C

85655588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 75327025-A-G

85655647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 75327087-G-A

85655680-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 75327120-A-G

85655698-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 75327138-G-C

85655698-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 75327138-G-T

85655974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75327419-G-A

85655986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75327430-G-A

85656070-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75327513-A-G

85656217-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75327648-G-C

85656241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75327672-A-G

85656253-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75327684-T-C

85656348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75327757-A-G

85657298-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75328389-C-G

85657770-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75328837-G-T

http://identifiers.org/hco/15/GRCh38#85658064-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75329114-C-A

85658387-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75329420-T-C

85658485-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75329518-T-C

http://identifiers.org/hco/15/GRCh38#85658489-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75329522-C-A

85658489-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75329522-C-G

http://identifiers.org/hco/15/GRCh38#85658502-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75329532-C-A

85658502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75329532-C-T

http://identifiers.org/hco/15/GRCh38#85658507-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75329537-A-C

85658507-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75329537-A-T

85658510-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75329540-A-G

85658516-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75329546-C-G

85658516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75329546-C-T

85658541-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 75329572-A-G

85658541-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 75329572-A-T

85658545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 75329576-G-A

85658599-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75329630-T-G

85658607-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75329638-C-G

85658610-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75329641-G-C

85658610-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75329641-G-T

http://identifiers.org/hco/15/GRCh38#85658615-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75329643-A-C

85658615-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75329643-A-G

http://identifiers.org/hco/15/GRCh38#85658616-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75329644-C-A

85658616-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75329644-C-G

85658640-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75329669-T-C

85658675-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75329701-T-C

85658679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75329705-T-C

85659002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75330174-G-A

85659060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75330233-C-T

85659124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75330340-T-C

85659442-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75330739-A-T

85659612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75330891-G-A

85659716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75331001-G-A

85659724-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75331006-G-T

85659795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75331075-G-A

http://identifiers.org/hco/15/GRCh38#85660352-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75331402-C-A

85660400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75331421-A-G

85660427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75331442-G-A

85660575-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75331634-G-T

85660753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75331875-C-T

85661402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75332475-G-A

85661406-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75332479-T-C

85661848-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75332608-A-G

85661848-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75332608-A-T

http://identifiers.org/hco/15/GRCh38#85662565-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75333314-C-A

85662565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75333314-C-T

85662566-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75333315-T-G

85662589-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75333338-A-G

85662698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75333454-G-A

85662806-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75333546-T-G

85663591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75333998-G-A

85663632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75334039-C-T

85663747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75334149-C-T

85663777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75334177-C-T

85663844-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75334229-T-A

85664017-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75334329-G-C

85664059-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75334369-A-G

http://identifiers.org/hco/15/GRCh38#85664209-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75334517-A-C

85664225-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75334539-A-G

85664500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75334807-G-A

85664500-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75334807-G-T

85664547-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75334849-T-C

85664547-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75334849-T-G

85664605-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 75334904-C-G

85664666-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 75334965-A-G

85664712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 75335011-A-G

85664712-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 75335011-A-T

85669540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75336826-G-A

http://identifiers.org/hco/15/GRCh38#85669610-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75336861-C-A

85669610-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75336861-C-G

85669610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75336861-C-T

85669628-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75336870-T-G

85669670-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75336908-G-T

85669724-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 75336963-A-G

85669826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 75337065-G-A

85669849-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75337089-A-T

85669856-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75337096-T-A

http://identifiers.org/hco/15/GRCh38#85669925-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75337155-C-A

85669925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75337155-C-T

85670033-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75337261-A-G

85670222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75337458-G-A

85670222-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75337458-G-T

85670620-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75337689-T-A

85670719-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 75337774-G-C

85670780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 75337823-G-A

85670781-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 75337824-G-T

85671121-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75338356-C-G

85671233-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75338465-C-G

85672796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75339041-G-A

85675526-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75339439-C-G

85675558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75339471-G-A

85676363-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75339884-G-C

85676372-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75339893-T-C

85676386-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75339908-T-C

85676862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75340556-G-A

85676896-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75340590-A-G

85676943-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75340651-T-C

85677058-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 75340771-T-C

85677083-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 75340796-G-T

85677095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 75340808-C-T

85677195-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75340905-T-A

85677195-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75340905-T-G

85677514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75341218-G-A

85677514-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75341218-G-C

85677642-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75341310-G-T

85677849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75341466-C-T

85677944-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75341582-A-T

85678105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75341745-G-A

85679534-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75343189-G-A

85680119-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75343751-T-C

85680214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75343846-C-T

85681137-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75344229-A-G

85681143-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75344235-A-G

85681187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75344270-C-T

85681566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75344689-C-T

85681574-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75344697-T-G

85681617-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75344737-C-G

85681664-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75344782-A-T

85681688-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75344806-A-G

85681688-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75344806-A-T

85682074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75345305-G-A

85682074-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75345305-G-C

85682074-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75345305-G-T

85682305-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75345513-A-G

85682545-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75345773-T-A

85682551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75345782-A-G

85683033-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75346202-G-T

85684056-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75346823-A-G

85684662-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75346984-A-G

85684762-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 75347071-T-C

85684777-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75347086-C-G

85684777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 75347086-C-T

http://identifiers.org/hco/15/GRCh38#85684929-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75347217-C-A

85684929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 75347217-C-T

85684962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 75347234-G-A

85684962-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 75347234-G-T

85684966-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 75347238-T-C

http://identifiers.org/hco/15/GRCh38#85684995-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75347267-C-A

85684995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 75347267-C-T

85685138-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 75347369-C-G

85685138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 75347369-C-T

85685226-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 75347422-C-G

85685226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 75347422-C-T

85685391-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 75347567-A-G

85685733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75347727-C-T

85685880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75347816-C-T

85686057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75347979-G-A

85686074-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75347996-A-T

85686506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75348835-G-A

85686648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75348948-G-A

85686689-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75348979-G-C

85687101-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75349322-A-T

85687132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75349353-C-T

85687403-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75349616-A-G

85688766-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75350583-T-A

85688771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75350588-G-A

85689094-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75350858-A-T

85689508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75351149-G-A

85689551-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75351192-T-C

85689975-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 75351774-A-G

85690266-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75352051-T-C

85690687-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75352511-A-G

85690772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75352591-G-A

85690856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75352669-C-T

85692004-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75353117-T-C

85692004-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75353117-T-G

85692012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75353126-G-A

85692140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75353248-G-A

http://identifiers.org/hco/15/GRCh38#85692222-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75353327-C-A

85692222-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75353327-C-G

85692609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75353535-C-T

85692711-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75353631-T-G

85692727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75353646-T-C

85692913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75353836-C-T

85693023-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75353911-G-T

85693228-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 75354065-A-G

85693356-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75354192-A-G

85693461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75354297-A-G

85693461-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75354297-A-T

85693516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75354356-G-A

85693566-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75354409-C-G

85693566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75354409-C-T

85693567-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75354410-C-G

85693603-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75354428-A-G

85693603-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75354428-A-T

85693627-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75354452-C-G

85695700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75355279-C-T

85695972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75355571-C-T

85696147-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75355741-G-C

85696202-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75355794-G-A

85696214-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75355804-A-G

85696327-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75355872-T-G

85696441-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75355974-C-G

85701851-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75360998-T-A

85702369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75361260-G-A

85702420-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75361316-A-G

85702726-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75361990-G-T

85702821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75362072-C-T

85702848-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75362099-T-A

85704238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75363085-A-G

85704429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75363137-C-T

85704684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75363427-A-G

85704757-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75363669-G-T

http://identifiers.org/hco/15/GRCh38#85704798-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75363710-A-C

85706499-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75365277-G-C

85706509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75365287-G-A

85706767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75365521-C-T

85706837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75365587-C-T

85706959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75365704-C-T

85706971-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75365716-T-C

85707300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75366004-G-A

85707405-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75366108-A-G

85707994-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75367493-G-T

85707997-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75367496-C-G

85707997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75367496-C-T

85708094-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 75367594-T-C

85708100-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75367600-G-C

85708103-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75367603-A-G

85708107-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75367607-C-G

85708107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75367607-C-T

85708125-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75367625-G-C

85708125-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75367625-G-T

85708126-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75367626-G-C

85708126-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75367626-G-T

85708149-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75367687-G-T

85708222-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75367905-T-A

85708341-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75368118-C-T

85708573-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75368354-T-G

85708587-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75368368-A-G

85708711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75368434-C-T

85708822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75368512-A-G

http://identifiers.org/hco/15/GRCh38#85709241-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75368935-A-C

85709241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75368935-A-G

85709251-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75368945-T-C

85709305-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75368984-T-A

85709321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75369000-C-T

85709384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75369051-G-A

85709384-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75369051-G-T

85709401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75369067-C-T

85709584-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75369269-T-G

85709619-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75369300-A-G

85709931-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75369362-A-G

85710058-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75369429-T-G

85710207-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75369553-A-G

85710293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75369618-G-A

85710293-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75369618-G-T

85710336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75369661-A-G

85710339-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75369664-G-T

85710414-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75369749-T-C

85710426-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75369761-A-T

85710506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 75369789-G-A

85710506-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 75369789-G-T

http://identifiers.org/hco/15/GRCh38#85710558-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#75369855-A-C

85710558-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 75369855-A-T

85710611-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 75369909-A-G

85710671-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75369966-T-G

85710689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75369984-G-A

85710689-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75369984-G-T

85710696-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75369991-A-G

85710799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75370109-C-T

85710823-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75370135-A-G

http://identifiers.org/hco/15/GRCh38#85710833-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75370145-C-A

85710833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75370145-C-T

85710947-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75370250-A-G

85710977-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75370280-T-C

85710997-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75370300-C-G

85711570-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75371078-A-G

85711588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75371095-A-G

85711831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75371294-G-A

85712324-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75371467-T-A

85712376-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75371504-T-C

85712415-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75371534-T-C

85713288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75372574-C-T

85713311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75372616-C-T

85713625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75372854-C-T

85715711-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75373445-G-T

85715721-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75373457-T-C

85715722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75373458-G-A

85715767-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75373508-G-T

85715943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75373684-G-A

http://identifiers.org/hco/15/GRCh38#85715985-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75373725-C-A

85715985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75373725-C-T

85716320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75373818-G-A

85716767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75374316-A-G

85716786-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75374335-T-C

85716829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75374397-A-G

85716850-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75374420-A-G

85717044-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75374824-T-A

85717054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75374832-C-T

http://identifiers.org/hco/15/GRCh38#85717264-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75375023-A-C

85717264-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75375023-A-G

85717332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 75375090-G-A

85717332-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 75375090-G-C

85717371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 75375129-C-T

85717416-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75375174-A-G

85717470-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75375222-A-G

85717470-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75375222-A-T

http://identifiers.org/hco/15/GRCh38#85717512-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75375261-C-A

85717512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75375261-C-T

http://identifiers.org/hco/15/GRCh38#85717638-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75375383-A-C

85717893-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75375597-T-C

http://identifiers.org/hco/15/GRCh38#85717914-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75375627-A-C

http://identifiers.org/hco/15/GRCh38#85717921-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75375634-C-A

85717964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75375669-G-A

85717989-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75375698-A-T

85718122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 75375831-A-G

85718207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75375914-G-A

85718693-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75376537-G-T

http://identifiers.org/hco/15/GRCh38#85718841-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75376594-A-C

85718841-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75376594-A-G

85719021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75376692-G-A

85719021-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75376692-G-C

85719021-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75376692-G-T

85719060-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75376702-T-G

85719239-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75376881-G-T

85719242-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 75376884-T-A

85719336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75376978-G-A

85719374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75377017-G-A

85719387-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75377030-T-G

85719471-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75377105-G-C

85719471-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75377105-G-T

85720411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75377377-T-C

85720761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75377834-C-T

85720822-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75377887-T-C

85720899-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75377960-T-C

85720931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75377991-G-A

85721185-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75378214-T-G

85721848-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75378390-A-G

http://identifiers.org/hco/15/GRCh38#85721858-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75378399-C-A

85721858-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75378399-C-G

85721907-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75378465-T-A

85721930-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75378488-A-G

85721930-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75378488-A-T

85721961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75378514-G-A

85721999-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 75378552-T-A

85721999-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 75378552-T-C

85722127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75378680-G-A

85722165-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75378719-T-C

85722199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75378751-G-A

85722199-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75378751-G-T

85722201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75378753-T-C

http://identifiers.org/hco/15/GRCh38#85722421-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75378945-C-A

85722425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75378949-G-A

85722447-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75378971-T-A

85722451-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75378975-T-A

85722561-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75379665-T-G

85722673-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75379765-G-C

85722767-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75379862-A-T

85722786-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75379881-T-G

85722949-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75379999-G-T

http://identifiers.org/hco/15/GRCh38#85722965-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75380015-A-C

85722965-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75380015-A-G

http://identifiers.org/hco/15/GRCh38#85722970-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75380020-C-A

85722970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75380020-C-T

85722983-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75380033-G-C

http://identifiers.org/hco/15/GRCh38#85723012-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75380053-C-A

85723012-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75380053-C-G

85723041-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75380081-A-G

85723041-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75380081-A-T

85723056-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75380095-A-G

85723057-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75380096-T-C

85723066-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 75380105-T-A

85723113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 75380152-C-T

85723274-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 75380313-A-G

85723277-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 75380316-T-G

85723301-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 75380340-T-C

http://identifiers.org/hco/15/GRCh38#85723324-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75380363-A-C

85723352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75380382-G-A

http://identifiers.org/hco/15/GRCh38#85723364-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75380394-C-A

85723364-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75380394-C-G

http://identifiers.org/hco/15/GRCh38#85723435-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75380409-C-A

85723435-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75380409-C-G

85723647-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75380472-T-G

85723713-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75380525-T-G

85723877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75380666-A-G

http://identifiers.org/hco/15/GRCh38#85723925-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75380710-A-C

85724104-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75380902-G-C

85724122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75380921-G-A

85724242-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75381016-T-G

85724243-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75381017-T-C

85724627-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75381330-A-G

http://identifiers.org/hco/15/GRCh38#85725023-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75381758-C-A

85725214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75381942-G-A

85725214-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75381942-G-C

85725348-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75382075-T-C

85725349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75382076-C-T

85725556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75382257-A-G

85725938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75384086-T-C

85725986-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75384124-T-C

85726392-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75385444-C-G

85726395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75385447-A-G

85726536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75385596-T-C

85726538-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75385598-A-G

85726672-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75385758-C-G

85726910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75385879-G-A

85726910-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75385879-G-T

http://identifiers.org/hco/15/GRCh38#85726967-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75385941-C-A

85726967-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75385941-C-G

85726967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75385941-C-T

85727016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75385986-G-A

85727323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75386274-G-A

85727323-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75386274-G-T

85727339-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75386287-A-G

85727370-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75386345-G-C

85727370-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75386345-G-T

85728222-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75387251-A-G

http://identifiers.org/hco/15/GRCh38#85728235-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75387259-A-C

85728741-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75387628-A-G

85729019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75387852-G-A

http://identifiers.org/hco/15/GRCh38#85729045-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75387878-A-C

85729045-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75387878-A-T

85730054-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75388748-T-C

85730269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75388926-G-A

85730355-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75388981-T-C

85730429-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, undefined
orthologous variants: 75389031-A-G

85730439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, undefined
orthologous variants: 75389041-G-A

85730439-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, undefined
orthologous variants: 75389041-G-T

http://identifiers.org/hco/15/GRCh38#85730475-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75389074-C-A

85730475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75389074-C-T

85730483-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75389082-A-G

85730485-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75389084-A-G

http://identifiers.org/hco/15/GRCh38#85730494-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75389091-C-A

85730494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75389091-C-T

85730607-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: synonymous variant
orthologous variants: 75389208-A-G

85730611-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: missense variant
orthologous variants: 75389212-G-T

85730682-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: synonymous variant
orthologous variants: 75389283-T-A

85730682-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: synonymous variant
orthologous variants: 75389283-T-C

85730725-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75389326-T-A

85730725-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75389326-T-C

85730729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75389330-C-T

85730806-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75389390-A-G

85730846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75389432-A-G

85730849-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75389435-T-A

http://identifiers.org/hco/15/GRCh38#85730853-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75389437-A-C

85730853-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75389437-A-G

85730855-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75389439-G-C

http://identifiers.org/hco/15/GRCh38#85730961-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75389544-C-A

85730987-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75389568-G-T

85734555-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75392039-G-T

85734720-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75392196-T-C

http://identifiers.org/hco/15/GRCh38#85734880-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75392268-C-A

85734880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75392268-C-T

85734964-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75392352-T-A

85734980-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75392372-C-G

85735185-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75392553-A-G

http://identifiers.org/hco/15/GRCh38#85735192-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75392557-A-C

85735192-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75392557-A-G

85735192-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75392557-A-T

85735196-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75392561-T-G

85735235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75392601-A-G

http://identifiers.org/hco/15/GRCh38#85735267-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75392637-A-C

85735267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75392637-A-G

85735271-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75392641-T-A

85735303-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75392671-C-G

85735362-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75392938-T-C

http://identifiers.org/hco/15/GRCh38#85735438-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75393099-C-A

85735438-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75393099-C-G

85735491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75393148-A-G

85735491-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75393148-A-T

85735547-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75393201-A-G

85735547-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75393201-A-T

85735653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75393315-A-G

http://identifiers.org/hco/15/GRCh38#85735694-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75393354-A-C

85735710-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75393370-A-T

http://identifiers.org/hco/15/GRCh38#85735734-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75393392-C-A

85735807-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75393432-A-G

85735823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75393448-C-T

85736032-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75393654-A-T

85736086-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 75393709-A-T

http://identifiers.org/hco/15/GRCh38#85736233-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75393821-C-A

85736233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75393821-C-T

85736352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75393910-A-G

85736387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75393951-G-A

85736448-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75393999-T-C

http://identifiers.org/hco/15/GRCh38#85736772-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75394254-A-C

85736780-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75394262-G-T

85737563-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75394721-T-A

85737674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75394803-G-A

85739978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75396264-C-T

85739980-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75396266-A-G

85740108-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75396373-A-G

85740186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75396439-C-T

85740303-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 75396587-T-C

85740339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 75396622-G-A

85740339-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 75396622-G-T

85740354-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 75396637-G-T

85740359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 75396642-G-A

85740359-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 75396642-G-T

85740406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 75396679-G-A

85740406-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 75396679-G-T

85740584-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75396748-T-A

85740678-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75396827-T-A

85740678-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75396827-T-C

85740678-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75396827-T-G

85740852-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75397149-G-C

85740895-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75397179-G-T

85740908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75397194-G-A

85740908-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75397194-G-T

85740930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75397218-G-A

85740930-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75397218-G-T

85740974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75397252-G-A

85740974-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75397252-G-C

85740974-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75397252-G-T

85740990-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75397270-G-T

85741123-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: synonymous variant
orthologous variants: 75397403-G-A

85741126-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: synonymous variant
orthologous variants: 75397406-C-G

85741132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: synonymous variant
orthologous variants: 75397412-G-A

85741156-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: missense variant
orthologous variants: 75397436-G-T

85741183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: synonymous variant
orthologous variants: 75397463-G-A

85741183-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: missense variant
orthologous variants: 75397463-G-T

85741210-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: missense variant
orthologous variants: 75397490-G-C

85742256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75398019-G-A

85742353-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75398068-A-G

85742604-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75398256-C-G

85742604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75398256-C-T

http://identifiers.org/hco/15/GRCh38#85742655-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75398303-C-A

85742655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75398303-C-T

85742656-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75398304-A-G

85742704-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, undefined
orthologous variants: 75398352-A-G

85742726-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75398374-G-A

85742732-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75398380-G-C

85742780-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75398428-T-C

http://identifiers.org/hco/15/GRCh38#85742923-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75398556-A-C

85742923-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75398556-A-G

85743288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75398833-C-T

85743594-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: synonymous variant
orthologous variants: 75399030-T-C

http://identifiers.org/hco/15/GRCh38#85743922-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75399302-C-A

85743922-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75399302-C-G

85743922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75399302-C-T

85744086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75399892-C-T

85744092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: 75399898-T-C

http://identifiers.org/hco/15/GRCh38#85744102-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75399906-A-C

85744124-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 75399928-C-G

85744124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 75399928-C-T

85744160-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 75399965-T-C

85744230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 75400035-G-A

85744333-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 75400101-T-A

85744581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 75400288-G-A

85744630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 75400324-G-A

85744630-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 75400324-G-C

85744630-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 75400324-G-T

85744732-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 75400420-C-G

85744732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 75400420-C-T

85744737-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 75400425-T-C

85744737-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 75400425-T-G

85744834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75400520-T-C

http://identifiers.org/hco/15/GRCh38#85745054-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75400729-A-C

85745054-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75400729-A-G

85745054-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75400729-A-T

85745074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75400753-A-G

85745129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75400795-G-A

85745129-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75400795-G-C

85745150-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75400815-A-G

85745150-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75400815-A-T

85745199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75400864-G-A

85745218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75400884-A-G

85745256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75400922-C-T

http://identifiers.org/hco/15/GRCh38#85745257-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75400923-C-A

85745257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75400923-C-T

85745279-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75400943-T-C

85745279-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75400943-T-G

85745317-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75400980-A-G

85745373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75401036-G-A

85745373-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75401036-G-T

85745447-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75401090-A-G

85745546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75401187-G-A

85745701-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75401279-G-A

http://identifiers.org/hco/15/GRCh38#85745735-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75401298-C-A

85745735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75401298-C-T

85745774-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75401336-G-T

85745910-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75401448-A-G

http://identifiers.org/hco/15/GRCh38#85745917-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75401455-C-A

85745917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75401455-C-T

85745979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75401508-T-C

85746014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75401543-G-A

85746014-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75401543-G-T

85746033-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75401562-A-G

http://identifiers.org/hco/15/GRCh38#85746100-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75401627-C-A

85746100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75401627-C-T

85746329-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75401848-G-T

85746415-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75401910-G-C

85746479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75401965-G-A

85746479-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75401965-G-C

85746479-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75401965-G-T

85746554-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75402036-G-T

85746620-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75402108-T-G

85746712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75402228-A-G

http://identifiers.org/hco/15/GRCh38#85746718-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75402234-C-A

85746718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75402234-C-T

85746749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75402261-G-A

85746778-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75402296-T-C

85746864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75402435-T-C

85747014-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75402541-A-T

85747091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75402600-G-A

85747334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75402791-G-A

85747334-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75402791-G-T

85747364-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75402817-T-C

85748081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75403453-G-A

85748119-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75403487-T-C

85748198-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75403537-T-A

85748214-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75403553-A-G

85748216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75403555-G-A

85748216-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75403555-G-T

85748339-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75403565-T-C

85748358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75403573-C-T

85748402-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75403603-A-G

http://identifiers.org/hco/15/GRCh38#85748504-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75403651-A-C

85748504-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75403651-A-G

http://identifiers.org/hco/15/GRCh38#85748545-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75403670-C-A

85748621-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75403727-A-G

85748654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75403758-G-A

85748654-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75403758-G-C

85748654-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75403758-G-T

http://identifiers.org/hco/15/GRCh38#85748690-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75403780-A-C

http://identifiers.org/hco/15/GRCh38#85748734-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#75403825-C-A

85748767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75403860-A-G

http://identifiers.org/hco/15/GRCh38#85748830-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#75403901-C-A

85748840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 75403911-G-A

85748840-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 75403911-G-T

http://identifiers.org/hco/15/GRCh38#85748928-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#75404003-C-A

85748928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 75404003-C-T

85748968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 75404029-G-A

85748968-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 75404029-G-C

85748968-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 75404029-G-T

85749062-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 75404062-C-G

85749123-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 75404127-A-G

85749277-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 371
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75404277-T-A