159865179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43791942-C-T

http://identifiers.org/hco/5/GRCh38#159865293-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#43791821-C-A

http://identifiers.org/hco/5/GRCh38#159865334-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#43791780-C-A

159865334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43791780-C-T

159865369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43791745-G-A

159865370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43791744-G-A

159865371-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43791743-A-G

159865372-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43791742-A-G

159865386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43791728-C-T

159865492-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43791628-C-G

159865711-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43791422-T-A

159865832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43791296-G-A

159866611-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43791047-T-A

159866631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43791027-G-A

159866893-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43790778-A-G

159866893-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43790778-A-T

159866914-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43790757-T-A

159866933-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43790738-G-T

159866945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43790726-G-A

159866945-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43790726-G-T

http://identifiers.org/hco/5/GRCh38#159866961-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#43790710-C-A

159866961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43790710-C-T

http://identifiers.org/hco/5/GRCh38#159867025-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#43790437-C-A

159867025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43790437-C-T

159867098-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43790366-G-A

159867098-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43790366-G-T

159867206-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43790268-C-G

159867248-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43790226-C-G

159867248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43790226-C-T

159867407-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43789860-T-G

159867498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43789779-C-T

159872660-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43787999-T-G

159872676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43787983-G-A

159872770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43787892-T-C

159873348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43787841-G-A

159873643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43787578-T-C

159873643-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43787578-T-G

159873731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43787500-A-G

159873835-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43787424-G-C

159873835-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43787424-G-T

159873868-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43787398-T-G

159873882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43787384-C-T

http://identifiers.org/hco/5/GRCh38#159873960-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#43787308-C-A

159874212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43786647-C-T

159874636-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43786217-A-T

159876429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43784475-C-T

159876526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43784379-G-A

159877040-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43783916-T-A

159877101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43783855-A-G

159877446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43783502-C-T

159877492-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43783458-G-C

http://identifiers.org/hco/5/GRCh38#159877672-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#43783337-C-A

159877700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43783306-C-T

159877715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43783292-G-A

159877901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43782974-C-T

159877924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43782806-C-T

http://identifiers.org/hco/5/GRCh38#159878305-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#43782440-C-A

159878552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43781628-G-A

159878777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43781411-G-A

159878777-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43781411-G-T

159878804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43781384-G-A

159878816-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43781373-A-T

159878838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43781351-G-A

159878838-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43781351-G-C

159878854-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43781335-C-G

159878936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43781237-C-T

159878955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43781219-T-C

159879051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43780848-C-T

159879173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43780733-C-T

159879311-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43780603-A-G

159879384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43780514-G-A

159880083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43780137-C-T

159880386-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43779867-T-G

159880466-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43779787-G-T

159880691-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43779178-T-C

159880807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43779053-G-A

159880969-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43778878-T-C

http://identifiers.org/hco/5/GRCh38#159880973-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#43778874-A-C

159880973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43778874-A-G

159880973-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43778874-A-T

http://identifiers.org/hco/5/GRCh38#159881236-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#43778781-C-A

159881283-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43778733-G-C

159881327-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43778691-C-G

159881362-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43778660-G-C

159881373-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43778651-T-A

159881373-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43778651-T-G

159881606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43778445-G-A

159881614-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43778437-T-A

159881620-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43778431-G-A

159881620-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43778431-G-C

159881620-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43778431-G-T

159881622-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43778429-T-C

159881629-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43778422-T-C

159881824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43777604-G-A

159881844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43777584-A-G

159882036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43777399-C-T

159882155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43777281-T-C

159882243-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43777175-G-C

159882293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43777127-G-A

159882767-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43776659-G-T

159882796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43776627-G-A

159882922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43776510-G-A

159882947-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43776482-A-G

159882971-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43776458-T-A

159883074-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43776360-G-C

http://identifiers.org/hco/5/GRCh38#159883075-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#43776359-C-A

159883253-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43776196-T-C

159883343-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43776121-T-C

159883364-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43776101-T-C

159883364-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43776101-T-G

159883382-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43776083-T-A

159883485-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43776007-T-A

159883485-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43776007-T-C

159883631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43775861-C-T

159883688-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43775804-A-G

159883752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43775738-G-A

159883819-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43775672-G-C

159883929-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43775561-T-C

http://identifiers.org/hco/5/GRCh38#159883953-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#43775537-C-A

http://identifiers.org/hco/5/GRCh38#159883976-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#43775515-C-A

159884919-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43774947-T-A

159884919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43774947-T-C

159885689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43769021-T-C

159885757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43768950-G-A

159885858-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43768857-T-C

http://identifiers.org/hco/5/GRCh38#159885975-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#43768679-A-C

159885975-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43768679-A-G

159886104-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43768549-A-G

159886233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43768440-G-A

159886409-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43768272-A-G

159886527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43768174-G-A

159886557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43768150-C-T

159886709-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43768017-T-C

159886738-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43767991-T-C

159886971-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43767149-T-C

159886986-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43767137-T-C

159887001-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43767122-T-C

159887062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43767053-C-T

159887106-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43767009-T-C

159887526-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43766613-A-G

159887849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43766414-G-A

159887918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43766350-G-A

159887918-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43766350-G-C

159887918-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43766350-G-T

http://identifiers.org/hco/5/GRCh38#159887919-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#43766349-C-A

159887919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43766349-C-T

http://identifiers.org/hco/5/GRCh38#159887937-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#43766331-C-A

159888069-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43766216-G-T

http://identifiers.org/hco/5/GRCh38#159888092-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#43766191-C-A

159888149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43766134-G-A

159888191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43765627-C-T

159888264-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43765561-G-T

159888286-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43765548-G-T

159888540-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43765327-A-G

159888977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43765105-C-T

159888998-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43765092-T-C

159889025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43765065-G-A

159889025-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43765065-G-T

159889190-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43764938-C-G

159889803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43764404-C-T

159889853-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43764356-G-A

159890012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43764204-G-A

http://identifiers.org/hco/5/GRCh38#159890540-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#43763700-C-A

159890744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43763497-G-A

http://identifiers.org/hco/5/GRCh38#159890841-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#43763416-A-C

159891017-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43763245-T-G

http://identifiers.org/hco/5/GRCh38#159891029-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#43763233-C-A

159891087-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43763162-T-A

159891192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43763057-C-T

159891223-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43763025-T-C

159891348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43762890-A-G

159891743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43762522-G-A

159891785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43762479-G-A

159893705-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43760833-A-G

159893738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43760802-G-A

159893826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43760716-G-A

159893891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43760654-G-A

159893926-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43760621-A-G

159894300-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43760294-C-G

159894460-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43760133-C-G

159894818-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43759429-A-G

159898410-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43758510-T-C

159898482-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43758368-T-C

159898482-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43758368-T-G

159900732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43753295-C-T

159900741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43753286-G-A

http://identifiers.org/hco/5/GRCh38#159900895-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#43753146-C-A

http://identifiers.org/hco/5/GRCh38#159901203-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#43752934-A-C

159902000-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43745120-A-T

159902549-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43744451-A-G

159902703-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43744300-C-G

159902749-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43744232-G-T

159902780-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43744197-T-C

159902997-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43743981-T-C

http://identifiers.org/hco/5/GRCh38#159903019-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#43743959-C-A

159903019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43743959-C-T

http://identifiers.org/hco/5/GRCh38#159903111-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#43743868-C-A

159903353-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43743622-T-C

159903396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43743584-C-T

159903546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43743427-C-T

159903557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43743416-T-C

159903681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43743286-C-T

159903825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43743170-C-T

159903889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43743129-C-T

159903901-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43743117-A-T

159904013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43742933-C-T

159904024-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43742922-A-G

159904143-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43742817-G-T

159904833-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43742261-A-G

159905242-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43741905-A-G

159905351-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43741821-A-G

159906422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43739783-G-A

http://identifiers.org/hco/5/GRCh38#159906473-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#43739726-C-A

http://identifiers.org/hco/5/GRCh38#159906643-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#43739560-C-A

159906795-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43739428-T-C

159906797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43739426-C-T

159906915-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43739339-T-A

159907265-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43738966-G-A

159907265-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43738966-G-T

159907520-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43738331-T-G

159907524-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43738327-T-A

159907533-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43738318-T-G

159907797-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43738059-G-A

159907820-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43738036-G-T

159907822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43738034-G-A

159907913-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43737945-T-C

159908104-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43737106-G-T

159908116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43737093-G-A

159908784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43735785-G-A

159908855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43735720-G-A

159908919-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43735662-A-G

159909148-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43735460-G-A

159909418-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43735194-G-C

159909418-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43735194-G-T

http://identifiers.org/hco/5/GRCh38#159909632-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#43734990-C-A

159909849-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43734772-G-C

159909849-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43734772-G-T

159909960-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43734643-T-A

159909960-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43734643-T-C

159910004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43734601-C-T

159910121-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43734344-A-T

159910203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43734264-G-A

159910402-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43734077-A-G

159910514-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43733968-A-G

159910588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43733904-A-G

159910651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43733839-C-T

http://identifiers.org/hco/5/GRCh38#159910745-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#43733727-C-A

159910892-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43733713-T-C

159911067-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43733624-T-G

159911619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43733259-C-T

http://identifiers.org/hco/5/GRCh38#159911760-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#43733129-C-A

159911831-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43733052-C-G

159911836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43733047-C-T

159912544-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43732365-C-G

http://identifiers.org/hco/5/GRCh38#159912583-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#43732326-C-A

159912583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43732326-C-T

159912687-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43732214-C-G

159912825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43732107-G-A

159912994-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43731933-C-G

159913273-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43731495-T-C

159913773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43730979-G-A

159914058-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43730719-T-G

159914066-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43730710-A-G

159914085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43730691-A-G

159914256-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43730531-G-T

159914534-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43730238-A-T

159914661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43730099-G-A

159914981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43729422-C-T

159915037-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43729130-T-G

159915064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43729103-G-A

159915190-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43728974-A-T

159915256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43728898-A-G

159915264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43728890-G-A

159915294-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43728859-A-G

http://identifiers.org/hco/5/GRCh38#159915378-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#43728780-A-C

159915785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43727988-C-T

159916040-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43727761-G-T

159916049-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43727753-G-C

159916054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43727748-G-A

159916054-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43727748-G-T

159916147-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43727651-A-G

159916240-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43727559-A-T

159916297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43727510-G-A

159916297-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43727510-G-T

http://identifiers.org/hco/5/GRCh38#159916554-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#43727263-C-A

159916554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43727263-C-T

159916595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43727221-C-T

159916713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 43727106-G-A

159916713-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 43727106-G-T

http://identifiers.org/hco/5/GRCh38#159916798-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#43727021-C-A

159916798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43727021-C-T

159916915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 43726904-G-A

159916915-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 43726904-G-T

http://identifiers.org/hco/5/GRCh38#159917161-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#43726658-A-C

159917198-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 43726621-T-A

159917198-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 43726621-T-C

159917233-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 43726586-T-C

159917466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 43726353-G-A

159917466-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 43726353-G-C

http://identifiers.org/hco/5/GRCh38#159917698-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#43726121-C-A

159917840-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 43725979-T-C

159917900-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43725926-T-C

159918366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43725473-G-A

159918795-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43725060-T-G

159919335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43724559-G-A

http://identifiers.org/hco/5/GRCh38#159919376-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#43724518-A-C

159919376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43724518-A-G

159919921-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43724044-A-G

159919991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43723974-G-A

159920427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43723601-C-T

159920448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43723580-A-G

159920481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43723543-G-A

159920693-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43723331-T-G

159920760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43723271-C-T

159921241-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43722799-T-A

159921241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43722799-T-C

159921241-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43722799-T-G

159921572-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43722481-G-C

http://identifiers.org/hco/5/GRCh38#159921877-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#43722188-C-A

159921877-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43722188-C-G

159922037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43722044-C-T

159922306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43721802-G-A

159922747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43721361-C-T

159922881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43721229-C-T

159922902-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43721212-A-G

159923018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43721118-G-A

http://identifiers.org/hco/5/GRCh38#159923104-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#43721058-C-A

159923128-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43721034-A-T

159923693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43719760-G-A

159923735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43719728-G-A

159923735-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43719728-G-T

http://identifiers.org/hco/5/GRCh38#159923785-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#43719679-C-A

159923800-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43719667-T-C

159923871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43719506-C-T

159924335-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43718914-T-C

159924508-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43718782-A-T

159924660-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43718636-C-G

159924786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43718552-G-A

http://identifiers.org/hco/5/GRCh38#159924814-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#43718523-C-A

159925017-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43718343-A-G

159925018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43718342-C-T

159925397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43718028-C-T

159925491-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 43717935-C-G

159929641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43716774-G-A

159929641-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43716774-G-T

http://identifiers.org/hco/5/GRCh38#159930771-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#43715224-A-C

159930862-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43715135-T-C

159931257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43714897-G-A

159931295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43714858-G-A

159931504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43714653-G-A

159931944-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43714280-A-G

159931947-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43714277-A-T

159932045-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43714193-A-G

159932640-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43713634-C-G

159932646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43713630-C-T

159932686-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43713573-A-G

159932759-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43713499-A-G

159932762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43713496-C-T

159932766-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43713492-A-G

159932787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43713471-A-G

159933387-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43712963-T-C

159933582-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43712735-C-G

159933994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43712132-C-T

159934303-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43711859-C-G

159934332-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43711826-A-G

159934432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43711728-G-A

159936464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43710806-G-A

159936819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43710398-G-A

159938300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: 43708918-G-A

159938301-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: 43708917-G-T

http://identifiers.org/hco/5/GRCh38#159938342-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#43708875-C-A

159938376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: 43708848-G-A

159938552-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: 43708682-G-T

159938579-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: 43708642-G-C

http://identifiers.org/hco/5/GRCh38#159938934-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#43708043-C-A

159939042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: 43707964-G-A

159939186-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: 43707862-G-T

159939248-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: 43707752-T-C

159939304-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: 43707696-T-A

159939304-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: 43707696-T-G

http://identifiers.org/hco/5/GRCh38#159939326-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#43707555-C-A

159939326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: 43707555-C-T

159939330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: 43707551-C-T

http://identifiers.org/hco/5/GRCh38#159939342-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#43707539-A-C

159939342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: 43707539-A-G

159939377-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: 43707513-T-C

159939405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: 43707480-G-A

159939405-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: 43707480-G-C

159939507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: 43707371-G-A

159940862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: 43704911-C-T

159943440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: 43703974-C-T

159943545-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: 43703885-T-A

159943546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: 43703884-T-C

159943818-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: 43703608-T-G

159943959-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: 43703504-T-A

159943959-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: 43703504-T-C

159944073-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: 43702828-T-C

159944416-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: 43702502-A-G

159944539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: 43702373-G-A

http://identifiers.org/hco/5/GRCh38#159944676-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#43702235-A-C

159944980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: 43701955-G-A

http://identifiers.org/hco/5/GRCh38#159945356-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#43701468-A-C

159945405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: 43701406-G-A

159945428-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: 43701367-G-C

159946227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: 43700146-C-T

159946371-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: 43700070-G-C

159946454-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: 43699995-G-T

159946455-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: 43699994-A-T

159946518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: 43699943-G-A

159947483-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: 43699128-A-G

159947559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: 43699053-T-C

159947596-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: 43699017-A-G

159947596-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: 43699017-A-T

159947769-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, missense_variant
orthologous variants: 43698843-T-A

159947783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, missense_variant
orthologous variants: 43698829-A-G

159947804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, missense_variant
orthologous variants: 43698808-C-T

159947829-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 43698782-T-C

159948089-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 43698533-T-C

159948108-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 43698514-T-A

http://identifiers.org/hco/5/GRCh38#159948574-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#43696168-C-A

http://identifiers.org/hco/5/GRCh38#159948589-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#43696153-A-C

159948631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 43696113-G-A

http://identifiers.org/hco/5/GRCh38#159948637-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#43696107-C-A

159948637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 43696107-C-T

159948646-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 43696098-T-A

159949364-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: 43693825-G-T

http://identifiers.org/hco/5/GRCh38#159949373-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#43693814-C-A

159949614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: 43693571-T-C

http://identifiers.org/hco/5/GRCh38#159949730-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#43693452-C-A

159949859-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: 43693335-T-A

159951728-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, undefined
orthologous variants: 43692824-T-C

159951916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: 43692648-G-A

http://identifiers.org/hco/5/GRCh38#159951987-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#43692583-A-C

159951987-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: 43692583-A-G

159952916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: 43690321-G-A

159952938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: 43690299-T-C

159953757-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: 43689600-T-A

159953894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: 43689459-A-G

159954013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: 43689397-C-T

159954051-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: 43689371-T-G

159954107-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: 43689329-A-G

159954245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: 43689098-C-T

159954390-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: 43688759-T-A

159954966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: 43687514-C-T

159954986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: 43687493-C-T

159954988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: 43687491-G-A

159955095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: 43687382-G-A

159955121-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, missense_variant
orthologous variants: 43687356-A-G

159955596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 43686891-G-A

159958203-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: 43683712-T-G

http://identifiers.org/hco/5/GRCh38#159958259-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#43683652-A-C

159958407-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: 43683534-G-T

http://identifiers.org/hco/5/GRCh38#159958520-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#43683442-C-A

159958929-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: 43683056-T-G

159958930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: 43683055-G-A

159959218-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: 43682773-G-C

159959542-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: 43682185-A-G

159959551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: 43682175-G-A

159959682-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: 43682043-A-G

159959682-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: 43682043-A-T

159960019-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: 43681749-G-T

159960126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: 43681681-G-A

159960772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: 43679641-G-A

159960785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: 43679628-G-A

159960890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: 43679512-C-T

159961433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: 43679093-C-T

159961560-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: 43678981-A-T

159961964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: 43678586-G-A

159961964-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: 43678586-G-T

159961969-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: 43678581-G-C

159963627-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: 43677392-G-C

159963813-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: 43677215-A-G

159963898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: 43677132-G-A

http://identifiers.org/hco/5/GRCh38#159963908-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#43677123-A-C

159963937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: 43677094-C-T

159963956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: 43677075-C-T

159964264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: 43676641-G-A

http://identifiers.org/hco/5/GRCh38#159964337-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#43676573-A-C

http://identifiers.org/hco/5/GRCh38#159964524-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#43675874-A-C

159964592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: 43675812-G-A

159965097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: 43675359-C-T

159965265-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: 43675213-A-G

159965367-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: 43675115-T-A

159965378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: 43675104-A-G

159965447-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: 43675038-G-C

159965594-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: 43674926-T-C

159965708-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: 43674795-T-C

159965725-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: 43674780-A-G

159965776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: 43674731-C-T

159965802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: 43674669-T-C

159966634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: 43673797-G-A

159966798-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: 43673638-T-C

http://identifiers.org/hco/5/GRCh38#159966875-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#43673547-A-C

159966876-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: 43673546-A-T

159966878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: 43673544-G-A

159966878-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: 43673544-G-T

159966906-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: 43673517-A-G

159966935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: 43673489-G-A

159967383-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: 43673074-T-C

159968464-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: 43671691-T-C

http://identifiers.org/hco/5/GRCh38#159968582-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#43671623-C-A

159968626-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: 43671619-A-G

159969006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: 43671407-G-A

http://identifiers.org/hco/5/GRCh38#159969049-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#43671365-C-A

159969237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: 43671207-A-G

http://identifiers.org/hco/5/GRCh38#159971852-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#43667304-C-A

159971852-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: 43667304-C-G

http://identifiers.org/hco/5/GRCh38#159971905-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#43667258-C-A

159971911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, missense_variant
orthologous variants: 43667252-G-A

159971911-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, missense_variant
orthologous variants: 43667252-G-C

http://identifiers.org/hco/5/GRCh38#159972031-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#43667132-C-A

159972031-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, missense_variant
orthologous variants: 43667132-C-G

159972031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, missense_variant
orthologous variants: 43667132-C-T

http://identifiers.org/hco/5/GRCh38#159972064-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#43667102-C-A

159972064-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, missense_variant
orthologous variants: 43667102-C-G

159972064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, missense_variant
orthologous variants: 43667102-C-T

159972076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, missense_variant
orthologous variants: 43667093-G-A

159972076-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, missense_variant
orthologous variants: 43667093-G-C

159972076-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, missense_variant
orthologous variants: 43667093-G-T

http://identifiers.org/hco/5/GRCh38#159972118-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#43667051-C-A

159972118-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 43667051-C-T

http://identifiers.org/hco/5/GRCh38#159972157-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#43667012-A-C

159972157-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, missense_variant
orthologous variants: 43667012-A-G

159972214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, missense_variant
orthologous variants: 43666955-G-A

159972214-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, missense_variant
orthologous variants: 43666955-G-C

159972214-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, missense_variant
orthologous variants: 43666955-G-T

159972247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, missense_variant
orthologous variants: 43666922-G-A

159972247-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, missense_variant
orthologous variants: 43666922-G-C

159972247-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, stop_gained
orthologous variants: 43666922-G-T

159972280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, missense_variant
orthologous variants: 43666892-G-A

159972280-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, missense_variant
orthologous variants: 43666892-G-C

159972280-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, missense_variant
orthologous variants: 43666892-G-T

159972283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, missense_variant
orthologous variants: 43666889-G-A

159972283-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, missense_variant
orthologous variants: 43666889-G-C

159972283-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, missense_variant
orthologous variants: 43666889-G-T

http://identifiers.org/hco/5/GRCh38#159972331-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#43666847-C-A

159972331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, missense_variant
orthologous variants: 43666847-C-T

159972362-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, missense_variant
orthologous variants: 43666816-T-A

159972362-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, missense_variant
orthologous variants: 43666816-T-C

159972370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, missense_variant
orthologous variants: 43666808-G-A

159972424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, missense_variant
orthologous variants: 43666754-G-A

159972424-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron_variant, missense_variant
orthologous variants: 43666754-G-T

http://identifiers.org/hco/5/GRCh38#159972508-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#43666672-C-A

159972508-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 43666672-C-G

159972511-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 43666669-T-C

159972511-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 43666669-T-G

http://identifiers.org/hco/5/GRCh38#159972512-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#43666668-C-A

159972512-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 43666668-C-G

159972512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 43666668-C-T

159972542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 43666635-G-A

159972542-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 43666635-G-T

159972585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 43666580-G-A

http://identifiers.org/hco/5/GRCh38#159972610-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#43666554-C-A

159972610-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 43666554-C-G

159972709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 43666457-G-A

159972723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 43666439-C-T

159972819-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 43666339-G-T

159972854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 43666304-G-A

159972860-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 43666298-T-A

159972893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 43666255-C-T

http://identifiers.org/hco/5/GRCh38#159972894-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#43666254-C-A

159972894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 43666254-C-T

159972897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 43666251-G-A

159972930-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 43666218-A-G

159975217-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: 43665204-A-T

159975421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: 43665008-G-A

159977009-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: 43662341-G-C

159977027-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: 43662325-A-T

159977224-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: 43661375-A-G

http://identifiers.org/hco/5/GRCh38#159977396-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#43661191-A-C

159977464-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 278
most severe consequence: intron variant
orthologous variants: 43661124-A-G