http://identifiers.org/hco/16/GRCh38#14833761-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#45683166-C-A

14833761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: 5 prime UTR variant
orthologous variants: 45683166-C-T

14833766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: 5 prime UTR variant
orthologous variants: 45683171-C-T

14833787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: 5 prime UTR variant
orthologous variants: 45683192-C-T

14833799-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: 5 prime UTR variant
orthologous variants: 45683204-T-C

http://identifiers.org/hco/16/GRCh38#14833944-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#45683324-C-A

14833947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: synonymous variant
orthologous variants: 45683327-G-A

14833947-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: synonymous variant
orthologous variants: 45683327-G-T

14833956-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: missense_variant, undefined
orthologous variants: 45683336-C-G

14834186-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45683481-T-C

14835215-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45684189-A-G

14835264-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron_variant, undefined
orthologous variants: 45684277-A-G

14835264-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron_variant, undefined
orthologous variants: 45684277-A-T

14835352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45684396-T-C

14835352-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45684396-T-G

14835442-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45684445-A-G

http://identifiers.org/hco/16/GRCh38#14835494-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#45684483-A-C

14835551-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45684551-T-G

14835603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45684603-C-T

14838116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45686695-G-A

14838249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45686827-G-A

14838249-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45686827-G-T

14838279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45686852-C-T

14838660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45687222-C-T

14838667-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45687227-G-C

http://identifiers.org/hco/16/GRCh38#14838779-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#45687337-C-A

14838779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45687337-C-T

14838798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45687355-C-T

14841131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45687752-G-A

14841258-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45687871-T-G

14841276-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45687887-T-G

14841283-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45687894-A-T

14841294-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45687905-C-G

14841294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45687905-C-T

14841321-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45687926-T-C

14841382-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: missense variant
orthologous variants: 45687987-T-G

14844663-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45690878-T-G

14844664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45690879-C-T

14844693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: synonymous variant
orthologous variants: 45690912-C-T

14844785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45691004-G-A

14846570-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 45691949-A-T

http://identifiers.org/hco/16/GRCh38#14846574-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#45691953-C-A

14846712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45692071-C-T

http://identifiers.org/hco/16/GRCh38#14846716-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#45692075-A-C

http://identifiers.org/hco/16/GRCh38#14846720-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#45692079-C-A

14846721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45692080-C-T

http://identifiers.org/hco/16/GRCh38#14846814-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#45692159-A-C

14846814-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45692159-A-G

14846814-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45692159-A-T

14846833-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45692176-G-T

http://identifiers.org/hco/16/GRCh38#14847423-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#45692410-A-C

14847467-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45692442-T-C

14847515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45692497-G-A

14847515-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45692497-G-C

14847758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45692740-G-A

14848890-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45693646-A-G

14849022-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45693768-A-G

14852377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45694635-G-A

14852501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45694756-T-C

14853149-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45695005-A-G

14853184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45695037-A-G

14853214-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45695064-T-G

14853255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45695084-C-T

14853256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 45695085-A-G

14853256-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 45695085-A-T

14853301-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45695128-A-T

http://identifiers.org/hco/16/GRCh38#14853391-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#45695213-A-C

14853391-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45695213-A-G

14853403-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45695224-A-G

14853559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45695365-T-C

14853780-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45696199-G-T

14853822-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45696238-T-C

http://identifiers.org/hco/16/GRCh38#14853827-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#45696243-C-A

14853892-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45696291-G-T

14853920-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45696316-C-G

14853942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45696338-G-A

14853942-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45696338-G-C

14853942-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45696338-G-T

http://identifiers.org/hco/16/GRCh38#14854038-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#45696436-C-A

14854081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45696473-A-G

http://identifiers.org/hco/16/GRCh38#14854654-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#45697112-C-A

14854654-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45697112-C-G

14854654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45697112-C-T

14854655-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45697113-A-T

14854698-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45697155-A-G

14854708-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45697165-G-C

http://identifiers.org/hco/16/GRCh38#14854769-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#45697213-A-C

14854769-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45697213-A-G

14855165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45697470-C-T

14855167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45697472-G-A

http://identifiers.org/hco/16/GRCh38#14855197-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#45697493-A-C

14855223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45697510-C-T

14855462-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45697679-A-T

14855751-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45697924-A-T

14856769-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45699270-C-T

14856815-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45699319-A-T

14856898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45699420-C-T

14857015-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45699538-T-C

14857088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45699592-G-A

14857088-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45699592-G-T

14857112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45699618-G-A

14857112-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45699618-G-T

14857113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45699619-C-T

http://identifiers.org/hco/16/GRCh38#14857167-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#45699660-C-A

14857167-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45699660-C-G

14857173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45699666-C-T

14857207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45699683-T-C

14857231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45699708-C-T

14857288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45699765-A-G

14857334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45699811-C-T

14857341-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45699818-C-G

14857341-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45699818-C-T

14857350-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45699828-A-G

14857409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45699875-G-A

http://identifiers.org/hco/16/GRCh38#14857430-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#45699896-A-C

14857471-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45699936-G-C

14857518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45699983-T-C

14857623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45700088-C-T

14858151-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45701299-C-G

14859059-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45701834-A-G

14860426-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45701926-T-C

14860526-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45702032-T-C

14860528-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45702034-G-A

14860788-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45702264-G-T

14860802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45702288-C-T

14862433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45703547-C-T

http://identifiers.org/hco/16/GRCh38#14862655-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#45703678-C-A

14862655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45703678-C-T

14862671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45703688-G-A

14862671-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45703688-G-T

14862885-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45703845-C-G

14862885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45703845-C-T

14863035-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45703948-T-A

14863052-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45703965-C-G

14863052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45703965-C-T

14863072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: missense variant
orthologous variants: 45703985-A-G

http://identifiers.org/hco/16/GRCh38#14863121-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#45704034-C-A

14863197-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45704112-A-G

14863540-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45704679-C-G

14863688-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45704803-C-G

14863709-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45704816-A-G

14864368-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45705602-C-G

14864368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45705602-C-T

14864465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45705696-G-A

14864465-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45705696-G-T

14864479-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45705710-C-T

http://identifiers.org/hco/16/GRCh38#14864505-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#45705736-A-C

14864505-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45705736-A-G

http://identifiers.org/hco/16/GRCh38#14864518-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#45705749-C-A

14864518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45705749-C-T

14864532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45705763-G-A

14864532-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45705763-G-C

14864532-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45705763-G-T

14864572-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45706006-C-G

14864683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: synonymous variant
orthologous variants: 45706117-T-C

14864744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45706178-A-G

14864755-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45706189-A-G

14864776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45706208-G-A

14864776-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45706208-G-T

14864781-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45706213-G-T

14864873-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45706316-T-C

14864990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45706467-G-A

14864990-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45706467-G-C

14865079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: synonymous variant
orthologous variants: 45706556-G-A

14865079-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: missense variant
orthologous variants: 45706556-G-T

14865097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: synonymous variant
orthologous variants: 45706574-C-T

14865359-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45706757-A-G

14865517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45706905-C-T

14865546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45706931-T-C

14865630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45707003-A-G

14867719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45709411-G-A

14867811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45709497-C-T

14867947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45709601-G-A

14867947-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45709601-G-T

14868046-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45709700-T-C

14868169-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45709806-T-C

14868256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45709888-G-A

14868314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45709899-A-G

14868477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45710061-G-A

14868643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 45710398-T-C

14868643-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 45710398-T-G

14871473-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45711054-T-C

14871474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45711055-G-A

14871474-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45711055-G-T

http://identifiers.org/hco/16/GRCh38#14871485-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#45711066-C-A

14871525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45711106-C-T

14871546-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45711132-C-G

14871546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45711132-C-T

14871554-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45711140-G-C

14871556-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45711142-T-G

14871561-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45711147-G-C

http://identifiers.org/hco/16/GRCh38#14871696-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#45711268-A-C

14871706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45711278-T-C

14871750-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45711319-T-G

14871753-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45711322-G-C

14871809-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45711393-A-G

14871953-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45711786-C-G

14871953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45711786-C-T

14872019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45711720-G-A

14872288-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: synonymous variant
orthologous variants: 45712445-T-G

14872339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45712496-G-A

14872345-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45712501-T-C

14872447-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45712539-T-C

14872536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45712583-G-A

14872577-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45712623-A-G

14872596-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45712645-G-T

14872895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45712880-G-A

14872900-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45712885-T-C

14873531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45713508-G-A

14873616-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45713597-G-T

14873679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45713635-T-C

14873704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45713658-G-A

14873704-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45713658-G-C

14873893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45713855-G-A

14873912-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45713874-A-G

14873931-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45713892-C-G

14873943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45713904-C-T

14874115-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron_variant, undefined
orthologous variants: 45714051-T-C

14874887-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45715436-C-G

14874887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45715436-C-T

http://identifiers.org/hco/16/GRCh38#14874894-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#45715443-A-C

14874981-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45715529-T-C

14874994-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45715542-C-G

14874994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45715542-C-T

14875000-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45715552-T-C

14875020-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45715570-G-C

14875297-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45715837-T-G

http://identifiers.org/hco/16/GRCh38#14875443-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#45715987-C-A

14875443-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45715987-C-G

14875443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45715987-C-T

14875484-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45716018-T-C

14875524-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45716061-G-T

14875567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45716096-G-A

14875567-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45716096-G-T

14875568-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45716097-G-T

14875572-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45716101-G-T

14876524-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45717969-C-T

14876615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45718048-G-A

14876702-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: missense variant
orthologous variants: 45718134-C-G

14876702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: missense variant
orthologous variants: 45718134-C-T

14876778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: synonymous variant
orthologous variants: 45718210-C-T

14876804-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45718229-T-C

14876817-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45718240-C-G

14876817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45718240-C-T

14876848-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45718271-A-G

14876849-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45718272-A-G

14878748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: missense variant
orthologous variants: 45719374-C-T

14878759-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: synonymous variant
orthologous variants: 45719385-C-G

14878759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: synonymous variant
orthologous variants: 45719385-C-T

14878864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45719474-T-C

14878899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45719489-G-A

14879143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45719688-C-T

14879199-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45719768-C-G

14879199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45719768-C-T

14879222-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45719798-A-G

http://identifiers.org/hco/16/GRCh38#14879233-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#45719809-C-A

14879233-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45719809-C-G

14879241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45719817-A-G

14879942-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45720140-C-G

14879942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45720140-C-T

14879975-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45720158-T-A

14879975-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45720158-T-G

14879977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45720160-G-A

14879977-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45720160-G-C

http://identifiers.org/hco/16/GRCh38#14880038-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#45720222-A-C

14880059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: synonymous variant
orthologous variants: 45720243-G-A

14880089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: synonymous variant
orthologous variants: 45720273-G-A

14880089-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: synonymous variant
orthologous variants: 45720273-G-T

14880151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45720335-C-T

14881466-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45721849-T-G

14881553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: synonymous variant
orthologous variants: 45721931-C-T

14881713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45722087-G-A

14881720-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45722088-T-G

14881732-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45722100-T-C

14881804-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45722155-C-G

http://identifiers.org/hco/16/GRCh38#14881814-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#45722162-C-A

14881814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45722162-C-T

14881822-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45722170-T-G

14882417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45725347-C-T

14882455-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45725374-G-C

http://identifiers.org/hco/16/GRCh38#14882548-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#45725463-C-A

14882548-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45725463-C-G

14882548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45725463-C-T

14882582-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45725487-G-T

14882611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: synonymous variant
orthologous variants: 45725516-C-T

14882659-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: synonymous variant
orthologous variants: 45725564-C-G

14884386-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: missense variant
orthologous variants: 45727464-C-G

14884386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: synonymous variant
orthologous variants: 45727464-C-T

14884392-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: synonymous variant
orthologous variants: 45727470-T-C

14885324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45727858-G-A

14885360-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45727894-C-G

http://identifiers.org/hco/16/GRCh38#14885462-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#45727976-C-A

14885463-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45727977-C-G

14885463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45727977-C-T

14885480-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45727993-A-G

14885501-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45728014-G-T

http://identifiers.org/hco/16/GRCh38#14885519-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#45728028-A-C

14885519-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45728028-A-G

14885558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45728058-G-A

14885583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45728092-C-T

14885644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45728149-G-A

14885663-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45728157-G-C

14885663-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45728157-G-T

14886027-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45728442-A-G

14886337-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45728611-G-C

14886337-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45728611-G-T

14886414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45728680-G-A

14886419-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45728685-T-C

14886738-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45728892-T-A

14886738-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45728892-T-C

14886746-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45728900-T-A

14886746-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45728900-T-C

http://identifiers.org/hco/16/GRCh38#14886767-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#45728921-C-A

14886778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: synonymous variant
orthologous variants: 45728932-C-T

14886882-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45729036-T-G

14886902-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45729047-T-C

14886971-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45729087-A-G

14886988-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45729105-A-G

14886996-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45729113-T-C

14887164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron variant
orthologous variants: 45729283-C-T

14888677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45730471-G-A

14888677-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45730471-G-T

14888681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45730475-G-A

http://identifiers.org/hco/16/GRCh38#14888706-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#45730500-C-A

14888706-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45730500-C-G

14888706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45730500-C-T

14888726-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45730515-G-A

14888726-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45730515-G-C

14888726-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45730515-G-T

http://identifiers.org/hco/16/GRCh38#14888732-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#45730521-C-A

14888732-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45730521-C-G

http://identifiers.org/hco/16/GRCh38#14888746-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#45730535-C-A

14888746-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45730535-C-G

14888746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45730535-C-T

14888758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45730546-A-G

14888758-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45730546-A-T

14888833-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45730618-G-T

14888885-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45730671-C-G

http://identifiers.org/hco/16/GRCh38#14888891-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#45730677-C-A

14888903-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45730689-A-T

http://identifiers.org/hco/16/GRCh38#14888906-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#45730692-C-A

14888906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45730692-C-T

14888975-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45730735-T-G

14889090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 45730813-G-A

14889101-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45730824-T-C

14889220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45730943-G-A

14889237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45730960-A-G

14889273-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45730982-T-G

14894775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45732480-C-T

14894780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45732485-G-A

14894884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45732555-G-A

14894884-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45732555-G-T

14894903-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45732573-C-G

14894903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45732573-C-T

14895006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45732667-G-A

http://identifiers.org/hco/16/GRCh38#14895018-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#45732679-C-A

14895018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45732679-C-T

14895024-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45732685-A-G

http://identifiers.org/hco/16/GRCh38#14895072-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#45732733-C-A

14895072-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45732733-C-G

14895072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45732733-C-T

14895103-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45732763-G-C

http://identifiers.org/hco/16/GRCh38#14895186-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#45732821-C-A

14895186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45732821-C-T

14895242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45732869-G-A

14895242-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45732869-G-T

14895332-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45732928-A-T

14895588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45733101-T-C

14895649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45733162-G-A

http://identifiers.org/hco/16/GRCh38#14895737-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#45733229-C-A

14895737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45733229-C-T

14895761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45733245-G-A

14895964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45733446-G-A

14895964-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45733446-G-C

14896056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45733524-T-C

14896065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45733533-C-T

14896076-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45733545-C-G

14896101-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45733570-T-C

14896105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30060
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45733573-C-T