http://identifiers.org/hco/10/GRCh38#122560838-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130633882-C-A

122560838-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 130633882-C-G

122560838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 130633882-C-T

122560839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 130633883-G-A

122560875-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron variant
orthologous variants: 130633922-A-G

122561034-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron variant
orthologous variants: 130634076-A-T

122561448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron variant
orthologous variants: 130634398-A-G

122561469-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron variant
orthologous variants: 130634420-C-T

http://identifiers.org/hco/10/GRCh38#122561471-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130634422-C-A

122561551-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron variant
orthologous variants: 130634477-T-C

http://identifiers.org/hco/10/GRCh38#122561569-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130634495-C-A

122561569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron variant
orthologous variants: 130634495-C-T

http://identifiers.org/hco/10/GRCh38#122561682-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130634566-A-C

122561682-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron variant
orthologous variants: 130634566-A-G

122561682-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron variant
orthologous variants: 130634566-A-T

122561871-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron variant
orthologous variants: 130634601-T-C

http://identifiers.org/hco/10/GRCh38#122562042-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130634673-A-C

122562042-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron variant
orthologous variants: 130634673-A-T

122562103-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron variant
orthologous variants: 130634725-G-T

122562216-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron variant
orthologous variants: 130634793-A-T

122562471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron variant
orthologous variants: 130634965-G-A

122562491-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron variant
orthologous variants: 130634985-C-G

122562528-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron variant
orthologous variants: 130635017-G-C

122562625-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron variant
orthologous variants: 130635089-G-C

122567290-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130665209-G-T

122567293-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130665212-C-G

122567311-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130665230-G-C

122567311-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130665230-G-T

122567318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130665237-A-G

http://identifiers.org/hco/10/GRCh38#122567322-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130665241-C-A

122567333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130665252-G-A

http://identifiers.org/hco/10/GRCh38#122567388-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130665302-C-A

122567429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130665353-G-A

122567429-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130665353-G-T

122567460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130638172-A-G

122567507-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130638237-C-G

http://identifiers.org/hco/10/GRCh38#122567527-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130638261-C-A

122567825-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130638530-G-C

122567908-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130638904-C-G

122567948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130638947-C-T

122567963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130638966-A-G

122567974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130638981-G-A

122568212-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130639190-A-T

122568384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130639361-C-T

122568406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130639374-G-A

122568638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130639595-C-T

122568640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130639597-G-A

122568744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130639701-A-G

122568928-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130639893-T-G

122569212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130640177-G-A

122569212-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130640177-G-T

122569321-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130640236-A-G

122569402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130640309-G-A

122569630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130640496-T-C

122569686-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130640553-A-G

122573206-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130647826-A-G

122573235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130647855-C-T

122573248-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130647868-G-C

122573328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130647940-C-T

122573333-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130647945-T-G

122573336-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130647948-T-G

122573408-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130648020-C-G

122573570-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130648164-A-G

122573574-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130648168-G-T

122573581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130648175-G-A

122573581-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130648175-G-T

http://identifiers.org/hco/10/GRCh38#122573605-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130648198-C-A

http://identifiers.org/hco/10/GRCh38#122573614-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130648207-C-A

122573614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130648207-C-T

http://identifiers.org/hco/10/GRCh38#122573615-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130648208-C-A

122573615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130648208-C-T

122573621-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130648214-T-C

122573636-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130648229-C-T

122573673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130640709-G-A

122573673-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130640709-G-T

122573817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130640832-G-A

122573817-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130640832-G-T

122573818-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130640833-T-G

122573848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130640862-G-A

122573867-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130640881-T-C

122573872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130640886-C-T

http://identifiers.org/hco/10/GRCh38#122573883-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130640894-C-A

122573883-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130640894-C-G

122573883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130640894-C-T

http://identifiers.org/hco/10/GRCh38#122573911-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130640920-C-A

122573916-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130640925-A-G

122573936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130640947-C-T

122573958-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130640976-T-C

122573982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130640996-C-T

122573994-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130641008-T-C

122573999-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130641013-T-C

122574136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130641119-C-T

http://identifiers.org/hco/10/GRCh38#122574199-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130641185-C-A

122574199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130641185-C-T

122574204-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130641190-G-T

http://identifiers.org/hco/10/GRCh38#122574243-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130641209-A-C

122574243-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130641209-A-G

122574260-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130641226-T-A

122574289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130641255-G-A

122574298-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130641264-G-C

122574298-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130641264-G-T

http://identifiers.org/hco/10/GRCh38#122574313-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130641278-C-A

122574313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130641278-C-T

122574315-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130641280-T-A

122574335-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130641299-G-C

122574357-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130641321-T-C

122574365-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130641329-T-C

122574420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130641384-C-T

122574452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130641409-G-A

122574477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130641433-G-A

122574477-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130641433-G-C

122574600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130641470-G-A

http://identifiers.org/hco/10/GRCh38#122574628-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130641499-A-C

122574628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130641499-A-G

122574628-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130641499-A-T

122575235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130674242-G-A

122575243-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130674250-A-G

122575267-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130674271-C-G

122575267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130674271-C-T

122575294-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130674298-T-C

122575295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130674299-G-A

122575295-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130674299-G-T

122575323-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130674327-G-T

122575350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130674386-G-A

122575351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130674387-C-T

http://identifiers.org/hco/10/GRCh38#122575365-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130674401-C-A

122575424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130674454-A-G

http://identifiers.org/hco/10/GRCh38#122575488-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130674522-A-C

122575488-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130674522-A-G

122575551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130674558-A-G

122575571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130674577-G-A

122575586-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130674592-A-G

http://identifiers.org/hco/10/GRCh38#122575658-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130674660-C-A

122575667-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130674669-T-C

122575683-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130674681-T-A

122576375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130642594-G-A

122576375-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130642594-G-C

122576400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 130642618-A-G

122576433-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 130642651-T-C

122576463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 130642681-G-A

122576487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 130642705-C-T

http://identifiers.org/hco/10/GRCh38#122576513-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130642731-C-A

122576513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 130642731-C-T

122576526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 130642744-C-T

http://identifiers.org/hco/10/GRCh38#122576634-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130651875-A-C

122576634-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 130651875-A-T

122576658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 130651899-C-T

122576661-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 130651902-C-G

122576661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 130651902-C-T

122576666-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 130651907-A-G

122576697-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 130651938-T-C

122576957-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130684692-C-G

122577036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130684775-C-T

122577051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130684791-G-A

122577147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130684881-C-T

http://identifiers.org/hco/10/GRCh38#122577171-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130684904-C-A

122577171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130684904-C-T

http://identifiers.org/hco/10/GRCh38#122577306-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130685044-A-C

122577341-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130685076-T-G

122577342-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130685077-G-C

122577349-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130685090-G-C

122577384-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130685120-G-T

http://identifiers.org/hco/10/GRCh38#122577535-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130685253-C-A

122577535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130685253-C-T

122577551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130685269-G-A

122577679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130685384-C-T

http://identifiers.org/hco/10/GRCh38#122577692-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130685396-C-A

122577692-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130685396-C-G

122577692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130685396-C-T

122577780-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130685486-G-C

http://identifiers.org/hco/10/GRCh38#122577820-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130685523-C-A

122577820-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 130685523-C-G

122579585-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 130659740-A-T

122579597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 130659752-C-T

122579608-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 130659763-T-C

122579642-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 130659797-G-C

122579672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 130659827-G-A

122579678-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 130659833-T-C

122579695-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 130659850-A-G

122579705-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 130659860-T-A

122579705-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 130659860-T-C

122579711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 130659866-C-T

122579725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 130659880-G-A

122579734-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 130659889-G-C

http://identifiers.org/hco/10/GRCh38#122579739-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130659894-A-C

122579739-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 130659894-A-G

122579769-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 130659924-C-G

122579770-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 130659925-A-G

http://identifiers.org/hco/10/GRCh38#122579774-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130659929-C-A

122579774-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 130659929-C-G

122579774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 130659929-C-T

122579780-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 130659935-A-G

122579798-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 130659953-T-C

http://identifiers.org/hco/10/GRCh38#122579814-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130659969-C-A

122579814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 130659969-C-T

122579816-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 130659971-T-A

122579816-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 130659971-T-C

122579816-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 130659971-T-G

122579828-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 130659983-G-C

122579828-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 130659983-G-T

http://identifiers.org/hco/10/GRCh38#122579834-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130659989-C-A

122579837-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 130659992-C-G

122579840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 130659995-C-T

122579873-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 130660028-T-C

122579873-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 130660028-T-G

122579928-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130708222-T-A

http://identifiers.org/hco/10/GRCh38#122579959-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130708250-C-A

122579960-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130708251-T-A

http://identifiers.org/hco/10/GRCh38#122579992-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130708283-C-A

122579992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130708283-C-T

122581083-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130685638-C-G

122586061-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, splice_region_variant, synonymous_variant
orthologous variants: 130675931-A-G

122586068-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, missense_variant
orthologous variants: 130675938-T-A

122586068-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, missense_variant
orthologous variants: 130675938-T-C

http://identifiers.org/hco/10/GRCh38#122586069-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130675939-C-A

122586069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, missense_variant
orthologous variants: 130675939-C-T

122586070-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 130675940-C-G

122586070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 130675940-C-T

122586071-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, missense_variant
orthologous variants: 130675941-A-T

122586079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 130675949-C-T

122586094-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 130675964-T-C

122586118-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 130675988-A-G

122586118-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 130675988-A-T

122586160-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 130676030-T-C

122586160-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, missense_variant
orthologous variants: 130676030-T-G

122586173-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, missense_variant
orthologous variants: 130676043-A-G

http://identifiers.org/hco/10/GRCh38#122586174-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130676044-C-A

122586174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, missense_variant
orthologous variants: 130676044-C-T

122586178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 130676048-T-C

122586187-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 130676057-T-C

122586199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 130676069-G-A

122586202-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 130676072-G-A

122586202-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, missense_variant
orthologous variants: 130676072-G-C

122586216-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, missense_variant
orthologous variants: 130676086-G-T

122586295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 130676165-G-A

122586295-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 130676165-G-C

122586319-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, missense_variant
orthologous variants: 130676189-C-G

122586319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 130676189-C-T

122586337-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 130676207-C-G

122586337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 130676207-C-T

122586390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 130676260-C-T

122586424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron variant
orthologous variants: 130684577-T-C

122586424-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron variant
orthologous variants: 130684577-T-G

http://identifiers.org/hco/10/GRCh38#122586429-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130684582-C-A

122586429-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron variant
orthologous variants: 130684582-C-G

http://identifiers.org/hco/10/GRCh38#122586476-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130684631-C-A

122586476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron variant
orthologous variants: 130684631-C-T

122586488-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron variant
orthologous variants: 130684651-T-C

http://identifiers.org/hco/10/GRCh38#122586533-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130684692-C-A

122586533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron variant
orthologous variants: 130684692-C-T

122588963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 130651659-C-T

122588974-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, missense_variant
orthologous variants: 130651670-T-C

122589044-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, missense_variant
orthologous variants: 130651740-T-A

122589058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, missense_variant
orthologous variants: 130651754-C-T

http://identifiers.org/hco/10/GRCh38#122589061-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130651757-A-C

122589061-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, missense_variant
orthologous variants: 130651757-A-G

122589071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 130651767-T-C

122589105-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, missense_variant
orthologous variants: 130651801-A-G

http://identifiers.org/hco/10/GRCh38#122589179-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130651875-A-C

122589179-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 130651875-A-G

122589186-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, missense_variant
orthologous variants: 130651882-T-C

http://identifiers.org/hco/10/GRCh38#122589200-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130651896-C-A

122589203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 130651899-C-T

http://identifiers.org/hco/10/GRCh38#122589206-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130651902-C-A

122589211-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, missense_variant
orthologous variants: 130651907-A-G

122589242-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, missense_variant
orthologous variants: 130651938-T-A

122592279-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 130659740-A-G

http://identifiers.org/hco/10/GRCh38#122592291-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130659752-C-A

122592291-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 130659752-C-G

122592291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 130659752-C-T

122592306-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 130659767-T-C

122592336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 130659797-G-A

122592336-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, missense_variant
orthologous variants: 130659797-G-C

122592366-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 130659827-G-C

122592372-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 130659833-T-C

122592389-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, missense_variant
orthologous variants: 130659850-A-G

122592419-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, missense_variant
orthologous variants: 130659880-G-T

122592432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 130659893-C-T

122592463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, stop_gained
orthologous variants: 130659924-C-T

122592464-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, missense_variant
orthologous variants: 130659925-A-G

122592468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 130659929-C-T

122592474-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 130659935-A-G

122592474-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 130659935-A-T

122592492-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 130659953-T-C

http://identifiers.org/hco/10/GRCh38#122592508-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130659969-C-A

122592508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, missense_variant
orthologous variants: 130659969-C-T

122592510-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, missense_variant
orthologous variants: 130659971-C-G

122592510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 130659971-C-T

122592518-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, missense_variant
orthologous variants: 130659979-A-T

122592522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 130659983-G-A

122592522-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 130659983-G-C

122592522-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 130659983-G-T

http://identifiers.org/hco/10/GRCh38#122592528-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130659989-C-A

122592531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 130659992-C-T

122592534-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 130659995-C-G

122592534-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 130659995-C-T

122592567-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, missense_variant
orthologous variants: 130660028-T-A

122592567-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, missense_variant
orthologous variants: 130660028-T-G

122592570-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: coding_sequence_variant, intron_variant, synonymous_variant
orthologous variants: 130660031-T-C

122592570-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: coding_sequence_variant, intron_variant, missense_variant
orthologous variants: 130660031-T-G

122592602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 130660063-C-T

122592608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron variant
orthologous variants: 130660069-G-A

122592609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron variant
orthologous variants: 130660070-A-G

http://identifiers.org/hco/10/GRCh38#122592611-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130660072-C-A

122592611-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron variant
orthologous variants: 130660072-C-G

122592611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron variant
orthologous variants: 130660072-C-T

122592626-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron variant
orthologous variants: 130660083-C-G

122592626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron variant
orthologous variants: 130660083-C-T

122592630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron variant
orthologous variants: 130660087-A-G

122592631-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron variant
orthologous variants: 130660088-C-G

122592631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron variant
orthologous variants: 130660088-C-T

122592633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron variant
orthologous variants: 130660090-G-A

122592635-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron variant
orthologous variants: 130660092-A-T

122592637-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron variant
orthologous variants: 130660094-T-C

122592637-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron variant
orthologous variants: 130660094-T-G

122592639-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron variant
orthologous variants: 130660096-T-C

122592641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron variant
orthologous variants: 130660098-C-T

http://identifiers.org/hco/10/GRCh38#122592643-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130660100-C-A

122592643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron variant
orthologous variants: 130660100-C-T

122598766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 130684209-C-T

122598838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 130684281-G-A

122598838-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, missense_variant
orthologous variants: 130684281-G-C

122598853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 130684296-C-T

122598874-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, missense_variant
orthologous variants: 130684317-T-A

122598874-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 130684317-T-C

122598891-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, missense_variant
orthologous variants: 130684334-A-G

122598892-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, missense_variant
orthologous variants: 130684335-T-A

122598892-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 130684335-T-C

http://identifiers.org/hco/10/GRCh38#122598904-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130684347-C-A

122598904-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 130684347-C-G

122598904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 130684347-C-T

122598913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 130684356-G-A

122598913-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, missense_variant
orthologous variants: 130684356-G-T

122598934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 130684377-C-T

http://identifiers.org/hco/10/GRCh38#122598935-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130684378-A-C

122598935-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, missense_variant
orthologous variants: 130684378-A-T

http://identifiers.org/hco/10/GRCh38#122598966-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130684409-A-C

122598970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 130684413-C-T

122598976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 130684419-A-G

122598976-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 130684419-A-T

122598994-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 130684437-T-C

122598994-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, missense_variant
orthologous variants: 130684437-T-G

122599164-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron variant
orthologous variants: 130668539-A-G

122599165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron variant
orthologous variants: 130668540-C-T

122599167-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron variant
orthologous variants: 130668542-T-C

122599169-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron variant
orthologous variants: 130668544-C-G

122599169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron variant
orthologous variants: 130668544-C-T

http://identifiers.org/hco/10/GRCh38#122599181-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130668556-C-A

122599181-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron variant
orthologous variants: 130668556-C-G

122599181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron variant
orthologous variants: 130668556-C-T

122601769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron variant
orthologous variants: 130675907-G-A

122601804-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 130675937-A-G

122601805-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, missense_variant
orthologous variants: 130675938-T-A

http://identifiers.org/hco/10/GRCh38#122601806-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130675939-C-A

122601806-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, missense_variant
orthologous variants: 130675939-C-G

122601807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 130675940-C-T

122601808-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, missense_variant
orthologous variants: 130675941-A-G

122601816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 130675949-C-T

122601911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, missense_variant
orthologous variants: 130676044-C-T

122601924-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 130676057-T-C

122601936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 130676069-G-A

122601936-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, missense_variant
orthologous variants: 130676069-G-T

122601939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 130676072-G-A

http://identifiers.org/hco/10/GRCh38#122602032-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130676165-A-C

122602032-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 130676165-A-G

122602047-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 130676180-G-C

122602056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 130676189-C-T

122602074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 130676207-C-T

http://identifiers.org/hco/10/GRCh38#122602127-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130676260-C-A

122602127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 130676260-C-T

122602133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron variant
orthologous variants: 130676266-G-A

http://identifiers.org/hco/10/GRCh38#122618036-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130651659-C-A

122618036-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: synonymous variant
orthologous variants: 130651659-C-G

122618036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: synonymous variant
orthologous variants: 130651659-C-T

122618051-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: missense variant
orthologous variants: 130651674-T-A

122618051-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: synonymous variant
orthologous variants: 130651674-T-C

122618068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: missense variant
orthologous variants: 130651691-G-A

122618068-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: missense variant
orthologous variants: 130651691-G-C

122618117-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: synonymous variant
orthologous variants: 130651740-T-C

122618130-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: missense variant
orthologous variants: 130651753-A-G

122618131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: missense variant
orthologous variants: 130651754-C-T

122618134-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: missense variant
orthologous variants: 130651757-A-G

122618144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: synonymous variant
orthologous variants: 130651767-C-T

122618156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: synonymous variant
orthologous variants: 130651779-G-A

122618156-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: missense variant
orthologous variants: 130651779-G-C

122618156-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: missense variant
orthologous variants: 130651779-G-T

http://identifiers.org/hco/10/GRCh38#122618178-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130651801-A-C

122618178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: missense variant
orthologous variants: 130651801-A-G

122618178-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: missense variant
orthologous variants: 130651801-A-T

122618252-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: synonymous variant
orthologous variants: 130651875-A-G

122618252-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: synonymous variant
orthologous variants: 130651875-A-T

122618259-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: missense variant
orthologous variants: 130651882-T-C

http://identifiers.org/hco/10/GRCh38#122618273-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130651896-C-A

122618273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: synonymous variant
orthologous variants: 130651896-C-T

122618279-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: synonymous variant
orthologous variants: 130651902-C-G

122618315-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: synonymous variant
orthologous variants: 130651938-T-C

122618318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: synonymous variant
orthologous variants: 130651941-A-G

http://identifiers.org/hco/10/GRCh38#122618364-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130708222-C-A

122618364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron variant
orthologous variants: 130708222-C-T

122618397-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron variant
orthologous variants: 130708249-A-T

http://identifiers.org/hco/10/GRCh38#122618398-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130708250-A-C

122618398-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron variant
orthologous variants: 130708250-A-G

122618399-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron variant
orthologous variants: 130708251-T-A

122618434-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron variant
orthologous variants: 130708283-T-C

http://identifiers.org/hco/10/GRCh38#122619200-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130709520-C-A

122619200-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron variant
orthologous variants: 130709520-C-G

122619200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron variant
orthologous variants: 130709520-C-T

122621030-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron variant
orthologous variants: 130659710-A-G

122621076-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 130659752-T-C

122621087-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, missense_variant
orthologous variants: 130659763-T-C

122621091-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 130659767-T-C

122621121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 130659797-G-A

122621121-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, missense_variant
orthologous variants: 130659797-G-T

122621151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 130659827-G-A

122621151-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 130659827-G-T

122621174-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, missense_variant
orthologous variants: 130659850-A-G

122621175-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 130659851-T-C

122621184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 130659860-T-C

122621190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 130659866-C-T

122621204-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, missense_variant
orthologous variants: 130659880-G-C

http://identifiers.org/hco/10/GRCh38#122621218-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130659894-A-C

122621253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 130659929-C-T

http://identifiers.org/hco/10/GRCh38#122621259-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130659935-A-C

122621277-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 130659953-T-C

http://identifiers.org/hco/10/GRCh38#122621293-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130659969-A-C

122621295-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 130659971-T-C

122621307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 130659983-G-A

122621316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 130659992-C-T

122621352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 130660028-T-C

http://identifiers.org/hco/10/GRCh38#122621355-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130660031-C-A

122621355-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 130660031-C-G

122621355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 130660031-C-T

122624553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130651659-C-T

122624564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130651670-T-C

122624639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130651754-C-T

122624642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130651757-A-G

122624686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130651801-G-A

122624787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130651902-G-A

122624787-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130651902-G-T

122624792-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130651907-A-G

122625286-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 130709623-T-G

122625914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130710165-G-A

122625920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130710171-T-C

122625920-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130710171-T-G

http://identifiers.org/hco/10/GRCh38#122633008-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130703505-C-A

http://identifiers.org/hco/10/GRCh38#122633009-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130703506-A-C

122633014-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron variant
orthologous variants: 130703515-T-G

http://identifiers.org/hco/10/GRCh38#122633025-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130703526-C-A

122633080-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron variant
orthologous variants: 130703573-T-C

122633096-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron variant
orthologous variants: 130703576-A-G

http://identifiers.org/hco/10/GRCh38#122633116-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130703596-A-C

122633198-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 130711221-T-C

122633532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130711486-G-A

122633564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130711519-G-A

122633708-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130711655-G-T

http://identifiers.org/hco/10/GRCh38#122634164-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130711934-C-A

122634186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130711957-C-T

122635888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130712582-G-A

122635888-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130712582-G-T

http://identifiers.org/hco/10/GRCh38#122635934-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130712619-C-A

122635934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130712619-C-T

122636063-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 130712722-T-G

122636079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 130712738-G-A

122636150-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 130712809-G-C

122636166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 130712825-G-A

122636166-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 130712825-G-C

122636235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130712897-G-A

122636235-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130712897-G-T

122636239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130712901-C-T

122636252-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130712913-T-C

122636279-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130712938-G-T

http://identifiers.org/hco/10/GRCh38#122636317-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130712997-C-A

122637037-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130713713-T-C

122637076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130713746-C-T

122637088-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130713757-G-C

http://identifiers.org/hco/10/GRCh38#122637106-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130713773-C-A

122637234-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 130713901-C-G

122637234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 130713901-C-T

122637429-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130714314-T-C

122637438-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130714320-T-A

122637438-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130714320-T-C

122638016-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130712722-C-G

122638903-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130716172-T-G

122639134-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130716539-A-T

122639934-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130718256-G-C

122639934-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130718256-G-T

http://identifiers.org/hco/10/GRCh38#122639990-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130718297-C-A

122640011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130718302-G-A

122640011-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130718302-G-T

122640035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 130718322-C-T

122640360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 130718626-T-C

http://identifiers.org/hco/10/GRCh38#122640578-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130718839-C-A

122640629-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130718877-C-T

122641137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130719250-G-A

122641172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130719268-C-T

122641204-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130719300-T-C

http://identifiers.org/hco/10/GRCh38#122641294-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130719393-C-A

122641416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130719491-G-A

http://identifiers.org/hco/10/GRCh38#122641613-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130719686-C-A

122642006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130720105-C-T

122642167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130720312-G-A

122642518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130720641-C-T

122642543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130720665-A-G

122642587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130720704-G-A

122642587-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130720704-G-T

122642987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130721041-T-C

http://identifiers.org/hco/10/GRCh38#122642997-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130721053-A-C

122642997-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130721053-A-G

http://identifiers.org/hco/10/GRCh38#122643023-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130721081-C-A

122643023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130721081-C-T

122643048-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130721104-T-C

122643048-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130721104-T-G

122643103-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130721115-G-T

122643218-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 130721232-C-G

122643218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 130721232-C-T

122643257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 130721271-G-A

122643257-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 130721271-G-C

http://identifiers.org/hco/10/GRCh38#122643404-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130721417-C-A

122643404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 130721417-C-T

http://identifiers.org/hco/10/GRCh38#122643406-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#130721419-C-A

122643406-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 130721419-C-G

122643406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 130721419-C-T

122643471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 130721490-G-A

122643471-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 130721490-G-T

122643664-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: 3 prime UTR variant
orthologous variants: 130721650-A-G

122643727-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2926
most severe consequence: 3 prime UTR variant
orthologous variants: 130721703-G-T