52362178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 20960846-G-A

52362178-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 20960846-G-C

52362178-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 20960846-G-T

52362289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20960945-G-A

52362289-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20960945-G-T

http://identifiers.org/hco/6/GRCh38#52362369-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#20961026-C-A

52362480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 20961134-G-A

52362480-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 20961134-G-C

52362480-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 20961134-G-T

52362503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20961163-G-A

52362508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20961168-G-A

52362508-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20961168-G-T

http://identifiers.org/hco/6/GRCh38#52362510-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#20961170-C-A

52362510-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20961170-C-G

52362510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20961170-C-T

52362544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20961198-G-A

52362544-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20961198-G-T

52362580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20961227-G-A

52362580-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20961227-G-T

52362584-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20961231-A-G

http://identifiers.org/hco/6/GRCh38#52362628-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#20961275-C-A

52362628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20961275-C-T

52362629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20961276-G-A

52362630-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20961277-G-T

52362636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20961283-G-A

52362636-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20961283-G-T

52363039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20961630-C-T

52363050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20961641-C-T

52363096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20961684-G-A

http://identifiers.org/hco/6/GRCh38#52363149-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#20961735-C-A

52363175-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20961763-T-G

52363407-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20961969-T-C

http://identifiers.org/hco/6/GRCh38#52363556-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#20962098-C-A

52363556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20962098-C-T

52363758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20962266-C-T

52363767-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20962275-G-T

52363872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20962359-G-A

52364055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20962496-T-C

52364055-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20962496-T-G

52364124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20962543-G-A

52364124-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20962543-G-T

52364145-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20962568-G-T

52364323-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20963207-A-G

52364495-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20963387-A-T

52364501-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20963393-A-G

52364552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20963444-G-A

52364761-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20963639-A-G

52364795-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20963672-G-T

52365321-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20964840-A-T

52365465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20965008-G-A

52365697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20965246-C-T

52365894-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20965406-G-T

52365930-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20965444-A-T

52366000-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20965691-T-C

52366158-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20965899-A-G

52366208-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20965940-A-G

52366264-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20965989-A-G

52368629-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20967787-A-G

52368694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20967852-A-G

52368695-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20967853-G-T

52368703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20967861-A-G

52369271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20970675-C-T

http://identifiers.org/hco/6/GRCh38#52369287-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#20970691-A-C

52369348-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20970756-A-T

52369571-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20970984-A-G

52369660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20971076-G-A

52369680-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20971106-T-A

52369694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20971125-A-G

52369716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20971147-G-A

52369900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20971312-A-G

52369972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20971384-G-A

52370004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20971411-C-T

52370352-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20971779-G-C

http://identifiers.org/hco/6/GRCh38#52370462-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#20971995-C-A

52370650-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20972188-G-C

52370795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20972314-C-T

52370815-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20972322-A-G

52370840-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20972342-C-G

52370943-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20972439-T-C

52371037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20972861-A-G

52371506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20973603-A-G

52371519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20973616-C-T

52371733-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20973802-A-T

52371838-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20973916-G-C

52372047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20974098-G-A

52372073-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20974122-G-T

52372107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20974174-G-A

52372107-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20974174-G-C

52372258-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20974343-T-C

52372260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20974345-G-A

52372368-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20974536-G-T

52372538-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20974698-A-G

52372912-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20975326-A-G

52372912-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20975326-A-T

52372965-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20975354-C-G

52373026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20975411-G-A

52373062-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20975446-A-G

52373439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20975991-A-G

52373457-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20976013-T-C

http://identifiers.org/hco/6/GRCh38#52373519-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#20976063-C-A

52373549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 20976092-G-A

52373549-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 20976092-G-T

http://identifiers.org/hco/6/GRCh38#52373568-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#20976111-C-A

52373568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20976111-C-T

52373642-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20976184-C-G

52373803-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20976345-G-C

52373829-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20976363-T-C

52375253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20977338-G-A

52375254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20977339-C-T

52375295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20977375-C-T

52375329-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20977409-A-G

52375562-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20977599-G-T

52375831-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20977831-T-C

52375916-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20977905-A-G

52376050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20978004-G-A

52376129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20978076-T-C

52376332-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20978296-T-C

52376360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20978324-G-A

52376398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20978361-G-A

52376471-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20978432-A-G

52376817-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20978803-C-G

52376817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20978803-C-T

52377047-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20979010-G-C

http://identifiers.org/hco/6/GRCh38#52377089-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#20979052-C-A

52377113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20979212-G-A

52377166-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20979265-T-C

52377166-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20979265-T-G

52377181-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20979280-T-G

52377339-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20979407-T-G

52377377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20979445-C-T

52377450-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20979513-T-C

52377467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20979525-G-A

http://identifiers.org/hco/6/GRCh38#52377810-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#20979713-A-C

52378390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20980389-G-A

http://identifiers.org/hco/6/GRCh38#52378394-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#20980394-A-C

52378394-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20980394-A-G

52380143-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20982822-A-G

52380206-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20982897-T-G

52380239-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20982929-G-T

http://identifiers.org/hco/6/GRCh38#52380281-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#20982973-A-C

52380341-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20983055-C-G

52380401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20983110-A-G

52380487-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20983197-G-T

52380536-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20983236-A-G

52380595-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20983348-T-C

52380795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20983549-G-A

52380816-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20983569-T-G

52381011-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20983767-C-G

52381078-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20983825-A-G

52381090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20983836-G-A

52381608-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20983967-G-C

52383806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20987901-C-T

52384183-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20988632-A-G

52384299-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20988728-T-G

52384320-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20988746-A-G

52388539-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20989804-G-C

52388862-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20990114-T-G

52388968-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20990221-T-G

52388972-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20990225-A-G

52389212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20990476-G-A

52389252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20990701-C-T

52389260-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20990766-T-G

52389486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20991047-C-T

52389590-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20991153-A-T

52389627-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20991190-G-T

52389650-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20991211-G-T

52390189-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20991722-T-A

52390767-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20992279-G-T

52390841-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20992352-T-G

52391079-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20992584-T-C

52391171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20992661-T-C

52391245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20992731-G-A

52391251-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20992736-T-C

52391283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20992760-C-T

52391794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20993235-G-A

52391942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20993383-T-C

52392042-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20993440-A-G

52392381-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20993513-A-G

52392470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20993585-C-T

52392493-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20993608-T-C

52392610-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20993723-G-C

52392691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20993823-G-A

52392691-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20993823-G-T

52392710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20993883-G-A

http://identifiers.org/hco/6/GRCh38#52394380-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#20994293-A-C

http://identifiers.org/hco/6/GRCh38#52395307-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#20994888-C-A

52395307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20994888-C-T

52395765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20996070-C-T

52396223-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20996436-A-T

52396617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20996819-G-A

52396628-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20996829-T-C

52396664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20996866-C-T

52396759-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20996957-A-G

52396865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20997060-A-G

52396966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20997161-G-A

52397023-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20997224-A-G

52397279-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20997558-T-C

52397482-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20997713-T-A

52397549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20997771-G-A

52397833-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20998037-T-A

52398004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20998215-C-T

http://identifiers.org/hco/6/GRCh38#52398007-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#20998218-C-A

52398007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20998218-C-T

52398117-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20999021-G-C

http://identifiers.org/hco/6/GRCh38#52398160-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#20999055-A-C

52398160-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20999055-A-T

52398165-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20999060-C-G

52398174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20999066-C-T

52398948-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20999195-T-C

52399130-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20999506-G-C

52399248-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20999628-G-T

52399282-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20999661-G-T

52399346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20999729-G-A

52399374-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20999753-C-G

52399400-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20999778-G-A

52399441-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20999815-G-C

52399470-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20999842-T-G

52399501-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20999873-A-G

52399526-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20999903-G-C

52399561-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20999938-C-G

52399646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21000021-C-T

52399755-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21001075-A-T

52399780-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21001102-A-G

52399829-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21001133-G-T

52399910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 21001215-G-A

52400029-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21001396-T-G

52400038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21001405-G-A

52400179-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21001529-A-G

52400247-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21001635-G-T

52400332-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21001683-T-C

52400493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21001842-C-T

52400782-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21002402-A-G

52401045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21002677-C-T

52401128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21002750-C-T

http://identifiers.org/hco/6/GRCh38#52401170-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#21002798-C-A

52401195-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21002823-A-G

52401376-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21002966-T-G

52401499-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21003109-A-G

52401546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21003156-T-C

52401559-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21003169-A-G

52401834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21004143-C-T

52403093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21004750-G-A

52403093-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21004750-G-T

52403164-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 21004808-T-C

52403165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21004809-G-A

52403165-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21004809-G-T

http://identifiers.org/hco/6/GRCh38#52403169-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#21004813-A-C

52403258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 21004892-C-T

52403285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 21004919-G-A

52403369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 21005003-C-T

52403474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 21005108-G-A

52403477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 21005111-C-T

http://identifiers.org/hco/6/GRCh38#52403559-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#21005193-A-C

52403559-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 21005193-A-G

52403562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 21005196-C-T

52403567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 21005201-G-A

52403609-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 21005243-G-T

52403735-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 21005369-G-T

52403738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 21005372-C-T

52403742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 21005376-C-T

52403798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 21005432-C-T

http://identifiers.org/hco/6/GRCh38#52404185-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: http://identifiers.org/mco/1/GRCm39#21005819-C-A

52404185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 21005819-C-T

http://identifiers.org/hco/6/GRCh38#52404351-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#21005989-C-A

52404351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21005989-C-T

52404460-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21006306-T-A

http://identifiers.org/hco/6/GRCh38#52404461-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#21006307-A-C

52404461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21006307-A-G

52404545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21006382-G-A

52404545-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21006382-G-T

52404547-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21006384-G-T

52404549-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21006386-A-G

52404560-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21006397-G-T

52404569-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21006406-T-A

52404615-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21006451-T-A

52404617-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21006453-A-T

http://identifiers.org/hco/6/GRCh38#52404618-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#21006454-A-C

52404618-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21006454-A-G

52404691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21006515-G-A

http://identifiers.org/hco/6/GRCh38#52404780-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#21006631-C-A

52404936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21006764-G-A

52404999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21006827-A-G

52405309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21007118-A-G

52405511-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21007312-T-C

52405538-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21007339-T-C

52405588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21007389-T-C

52405650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21007451-C-T

http://identifiers.org/hco/6/GRCh38#52405912-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#21007700-A-C

52405923-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21007711-A-G

52405956-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21007729-A-G

52406068-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21007838-G-T

52406087-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21007857-G-C

52406087-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21007857-G-T

52406138-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21007905-T-G

52406213-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21007983-T-C

http://identifiers.org/hco/6/GRCh38#52406255-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#21008024-C-A

52406255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21008024-C-T

52406297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21008070-G-A

52406297-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21008070-G-T

http://identifiers.org/hco/6/GRCh38#52406307-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#21008080-A-C

52406332-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21008093-C-G

52406332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21008093-C-T

52406778-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21008450-G-T

52406939-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21008631-G-T

52407227-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21008977-T-A

52407273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21009048-C-T

52407434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21009346-A-G

http://identifiers.org/hco/6/GRCh38#52407505-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#21009413-C-A

52407571-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 21009443-A-G

52407760-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21009597-A-G

52407773-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21009610-A-G

52407786-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 21009623-G-T

http://identifiers.org/hco/6/GRCh38#52407857-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#21009644-C-A

52407910-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21009700-A-G

52407918-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21009708-T-A

52408027-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21009764-A-G

52408076-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21009810-A-G

52408107-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21009840-G-C

52409888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21010088-C-T

52410103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21010308-C-T

52410203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21010406-A-G

52410453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21010654-C-T

52410468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21010710-G-A

52410471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21010713-T-C

52410533-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21010779-A-G

52410701-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21011009-C-G

http://identifiers.org/hco/6/GRCh38#52411115-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#21011645-C-A

52411342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21011855-G-A

http://identifiers.org/hco/6/GRCh38#52411438-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#21011955-C-A

52411598-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21012104-A-G

52411654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21012161-C-T

52411968-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21012407-T-C

52412027-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21012464-A-T

52412479-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21012554-C-T

52412480-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21012555-A-G

52412542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21012617-C-T

52412569-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21012644-T-C

52412599-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21012674-A-G

52412605-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21012680-T-A

52412688-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21012791-C-G

52412783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21012871-C-T

52412876-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21012947-C-G

52412889-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21012959-G-C

52412889-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21012959-G-T

52414353-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21013754-A-T

52414423-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21013845-A-T

52414680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21014385-C-T

52414880-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21014651-T-G

52414986-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21014758-T-C

52415102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21014850-C-T

52415208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21014936-C-T

52416566-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21017799-T-C

http://identifiers.org/hco/6/GRCh38#52416594-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#21017826-C-A

http://identifiers.org/hco/6/GRCh38#52416723-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#21017902-C-A

52416750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21017931-G-A

http://identifiers.org/hco/6/GRCh38#52416874-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#21018040-C-A

52417726-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21018934-G-T

http://identifiers.org/hco/6/GRCh38#52417784-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#21018989-A-C

52418458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21019298-A-G

52418655-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21019478-A-G

52418794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21019612-G-A

52418807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21019625-C-T

52418974-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21020869-T-A

http://identifiers.org/hco/6/GRCh38#52419017-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#21020910-C-A

52419068-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21020948-A-G

52419077-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21020957-G-T

http://identifiers.org/hco/6/GRCh38#52419143-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#21021021-A-C

52419165-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21021038-T-G

http://identifiers.org/hco/6/GRCh38#52419248-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#21021122-C-A

52419248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21021122-C-T

52419321-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21021191-A-G

http://identifiers.org/hco/6/GRCh38#52419350-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#21021219-C-A

52419726-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 21021291-G-C

52419726-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 21021291-G-T

52419747-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21021306-T-C

52419747-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21021306-T-G

52419753-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21021312-A-T

52419785-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 21021332-A-G

52419847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 21021397-C-T

52419849-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 21021399-A-G

http://identifiers.org/hco/6/GRCh38#52419854-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#21021404-C-A

52419854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 21021404-C-T

52419860-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 21021410-T-C

52419870-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 21021421-T-A

52419870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 21021421-T-C

52419881-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 21021432-A-G

52419936-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21021495-G-T

http://identifiers.org/hco/6/GRCh38#52419940-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#21021499-C-A

52419940-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21021499-C-G

http://identifiers.org/hco/6/GRCh38#52420017-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#21021545-C-A

52420017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 21021545-C-T

http://identifiers.org/hco/6/GRCh38#52420022-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#21021550-C-A

http://identifiers.org/hco/6/GRCh38#52420083-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#21021613-C-A

52420086-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 21021616-T-C

http://identifiers.org/hco/6/GRCh38#52420267-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#21021789-C-A

52420267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 21021789-C-T

http://identifiers.org/hco/6/GRCh38#52420274-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#21021797-C-A

52420274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 21021797-C-T

http://identifiers.org/hco/6/GRCh38#52420298-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#21021834-C-A

http://identifiers.org/hco/6/GRCh38#52420382-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#21021933-C-A

52420524-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21022034-A-G

52420594-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 21022084-C-G

52420594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 21022084-C-T

52420795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21022200-C-T

http://identifiers.org/hco/6/GRCh38#52420903-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#21022268-C-A

http://identifiers.org/hco/6/GRCh38#52420963-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#21022311-C-A

52420963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21022311-C-T

http://identifiers.org/hco/6/GRCh38#52420965-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#21022313-C-A

http://identifiers.org/hco/6/GRCh38#52421034-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#21022371-A-C

52421034-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 21022371-A-T

52421036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 21022373-G-A

52421036-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 21022373-G-T

http://identifiers.org/hco/6/GRCh38#52421050-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#21022387-C-A

52421050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 21022387-C-T

52421125-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 21022460-T-G

52421127-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 21022462-T-C

52421177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21022503-G-A

52421177-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21022503-G-C

52421177-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21022503-G-T

52421681-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21023716-A-G

52421733-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21023758-T-C

52422507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21024277-G-A

52422507-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21024277-G-T

52422676-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21024466-A-T

52422798-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21024601-A-G

52422809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21024615-G-A

52422875-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21024668-T-C

52423052-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21024877-G-T

52423178-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21024999-T-A

52423259-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21025062-T-G

52423392-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21025149-T-C

52423763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21025403-C-T

52423923-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 21025538-T-C

http://identifiers.org/hco/6/GRCh38#52423987-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#21025600-C-A

52423987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 21025600-C-T

52424019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 21025632-G-A

52424033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 21025646-C-T

52424053-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21025666-G-C

52424127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 21025740-C-T

http://identifiers.org/hco/6/GRCh38#52424218-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#21025835-C-A

52424218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 21025835-C-T

52424267-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21025864-C-G

52424267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21025864-C-T

52424289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 21025883-G-A

52424296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 21025890-C-T

http://identifiers.org/hco/6/GRCh38#52424297-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#21025891-C-A

52424297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 21025891-C-T

52426144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21026268-G-A

52426324-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21026404-T-A

52426376-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21026449-T-G

52426391-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21026464-T-C

52426455-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21026517-T-A

52426523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21026583-G-A

52426534-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21026594-G-A

52426572-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21026634-T-C

52426809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21026925-T-C

52428046-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21027003-T-C

52428084-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21027039-T-C

52435015-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21028565-G-T

52435025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21028575-G-A

52435856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21029384-T-C

52436079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21029581-C-T

http://identifiers.org/hco/6/GRCh38#52436198-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#21029701-C-A

52436401-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21029884-C-G

52436401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21029884-C-T

52438233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21030301-G-A

52438233-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21030301-G-T

52438427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 21030477-G-A

52438608-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21030657-T-G

52438663-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21030714-T-C

52438729-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21030773-G-T

52452173-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21031202-G-T

52452201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21031230-G-A

52452961-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21031621-T-C

52452983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21031632-G-A

52453055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21031899-C-T

52453056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21031900-G-A

52453069-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21031913-G-C

http://identifiers.org/hco/6/GRCh38#52453091-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#21031935-C-A

52453117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21031961-G-A

52453117-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21031961-G-T

52453146-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21031990-T-C

52453292-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21032603-G-C

52453316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21032627-G-A

52453316-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21032627-G-T

52453353-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21032664-A-G

http://identifiers.org/hco/6/GRCh38#52453401-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#21032701-A-C

52453432-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21032729-G-T

52453456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21032756-G-A

52453456-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21032756-G-T

52453545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21032841-G-A

http://identifiers.org/hco/6/GRCh38#52453548-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#21032847-C-A

52453548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21032847-C-T

http://identifiers.org/hco/6/GRCh38#52453554-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#21032853-A-C

52453563-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21032862-T-A

52453569-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21032866-A-T

52453573-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21032870-T-G

52453582-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21032877-T-A

52453582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21032877-T-C

52453587-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21032882-A-T

52454051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21037506-C-T

52454187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21037640-G-A

52454187-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21037640-G-C

52454208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21037661-C-T

52454296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21037749-G-A

52454296-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21037749-G-T

http://identifiers.org/hco/6/GRCh38#52454385-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#21037833-C-A

52454385-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21037833-C-G

52454385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21037833-C-T

52454391-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21037839-G-T

52454434-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21037867-T-C

52454465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21037898-G-A

52454652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 21038264-C-T

52454656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 21038268-C-T

52454678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 21038290-A-G

52464321-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21042065-G-T

52464351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21042099-G-A

52464357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21042105-A-G

52464435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21042182-G-A

52464714-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21042399-A-G

52464725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21042410-G-A

http://identifiers.org/hco/6/GRCh38#52464780-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#21042455-C-A

52464847-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21042956-G-T

52464981-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 21043085-C-G

52464981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 21043085-C-T

52465120-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21043224-T-G

52465139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21043243-G-A

52465146-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21043250-G-T

52465262-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21043331-A-G

52469299-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21045101-T-A

52478807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21048681-C-T

52478816-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21048690-A-G

52478827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21048706-G-A

52478847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21048726-G-A

52478872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21048751-G-A

52478909-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21048782-T-A

http://identifiers.org/hco/6/GRCh38#52478975-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#21048809-A-C

52478975-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21048809-A-T

http://identifiers.org/hco/6/GRCh38#52478982-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#21048816-C-A

52478982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21048816-C-T

52478983-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21048817-A-G

52478983-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21048817-A-T

52479240-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21049070-T-C

52479494-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21049339-A-G

52479504-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21049387-G-T

52479515-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21049508-A-G

52479548-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21049541-T-A

http://identifiers.org/hco/6/GRCh38#52479553-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#21049546-A-C

52479553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21049546-A-G

52479704-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21049698-C-T

52479705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 21049699-G-A

52479767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21049761-G-A

52479771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 21049765-G-A

52479771-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 21049765-G-C

52479771-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 21049765-G-T

52479773-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21049767-T-C

52479773-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21049767-T-G

52479798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 21049790-G-A

52479800-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 21049792-T-C

52480512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21050450-C-T

52480517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21050455-G-A

http://identifiers.org/hco/6/GRCh38#52480634-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#21050577-A-C

52480685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21050617-G-A

52480793-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21050709-A-G

52480852-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21050759-T-G

52480879-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21050794-T-A

52480879-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21050794-T-C

52480917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21050832-G-A

52485384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21055194-G-A

52486638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21055724-G-A

52486638-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21055724-G-C

52486722-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21055779-T-C

52486769-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21055807-A-G

52486882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21055890-T-C

52486970-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21056200-T-C

52487026-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21056259-A-T

52487050-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21056283-T-A

52487066-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21056289-C-G

52487092-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21056313-A-G

http://identifiers.org/hco/6/GRCh38#52487185-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#21056388-C-A

52487185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21056388-C-T

52487266-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21056461-T-G

52487344-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21056533-T-C

52487360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21056549-G-A

52487453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21056623-G-A

52487453-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21056623-G-T

http://identifiers.org/hco/6/GRCh38#52487483-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#21056666-A-C

52487591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21056759-C-T

52488009-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21057732-G-T

52488211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21057922-C-T

52488433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21058202-G-A

52488433-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21058202-G-T

52489558-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21059076-G-T

http://identifiers.org/hco/6/GRCh38#52489590-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#21059098-C-A

52489591-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21059099-T-G

http://identifiers.org/hco/6/GRCh38#52489606-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#21059114-C-A

52489606-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21059114-C-G

52489647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21059158-C-T

52489652-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21059163-C-G

52490011-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21059479-T-C

52490011-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21059479-T-G

52490023-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21059491-G-T

52490031-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21059496-G-C

52490031-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21059496-G-T

52490042-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21059505-A-G

http://identifiers.org/hco/6/GRCh38#52490068-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#21059531-A-C

52490083-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21059546-G-T

52490137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 21059589-C-T

52490154-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 21059631-A-G

52490180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 21059656-G-A

http://identifiers.org/hco/6/GRCh38#52490204-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#21059680-C-A

52490204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 21059680-C-T

52490238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 21059714-G-A

52490238-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 21059714-G-C

52490266-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21059742-A-G

52490266-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 21059742-A-T

52490313-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 21059789-C-G

52490313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 21059789-C-T

http://identifiers.org/hco/6/GRCh38#52490382-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#21059873-C-A

http://identifiers.org/hco/6/GRCh38#52490499-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#21059951-C-A

52490499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21059951-C-T

http://identifiers.org/hco/6/GRCh38#52490513-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#21059963-C-A

52490513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21059963-C-T

52490602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21060049-G-A

52490602-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21060049-G-T

52490797-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21060239-G-A

52490797-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21060239-G-T

52490799-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21060241-G-T

52490803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21060245-G-A

52490940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21060369-G-A

52491085-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21060511-G-T

52492075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21060622-C-T

http://identifiers.org/hco/6/GRCh38#52492139-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#21060687-C-A

52492161-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21060706-T-C

http://identifiers.org/hco/6/GRCh38#52492194-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#21060746-C-A

52492194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21060746-C-T

52492249-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21060806-T-C

52492249-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21060806-T-G

52492324-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 21060895-C-G

52492324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 21060895-C-T

52492358-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21060927-T-A

52492435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21060993-T-C

http://identifiers.org/hco/6/GRCh38#52492462-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#21061022-C-A

52492462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21061022-C-T

52492478-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21061038-A-G

52492480-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21061040-T-A

52492538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21061093-G-A

52492557-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21061112-T-A

52493863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21062018-G-A

52493878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21062033-G-A

52493916-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21062072-A-G

52495753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21064268-A-G

52495973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21064420-C-T

http://identifiers.org/hco/6/GRCh38#52496162-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#21064602-C-A

52496265-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21064680-T-C

52496712-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21065633-T-C

52496914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21065823-A-G

52496926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21065835-C-T

52496949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21065859-G-A

52496949-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21065859-G-T

52497298-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21066380-A-G

52497339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21066428-G-A

52497611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21066745-G-A

52497612-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21066746-T-C

52497612-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21066746-T-G

52497965-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21067102-T-C

52498022-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21067163-T-C

52498242-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21067388-G-T

52498274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21067420-G-A

52498609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21067775-C-T

http://identifiers.org/hco/6/GRCh38#52498625-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#21067791-C-A

http://identifiers.org/hco/6/GRCh38#52498695-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#21067858-C-A

52498695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21067858-C-T

http://identifiers.org/hco/6/GRCh38#52498702-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#21067865-C-A

52498904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21068077-G-A

52498992-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21068149-A-G

52499039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21068169-C-T

52499100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21068200-G-A

52499100-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21068200-G-T

http://identifiers.org/hco/6/GRCh38#52499119-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#21068222-A-C

52499119-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21068222-A-G

52499301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21068386-A-G

http://identifiers.org/hco/6/GRCh38#52499437-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#21068513-C-A

52499485-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21068563-A-G

52499486-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21068564-G-T

http://identifiers.org/hco/6/GRCh38#52499522-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#21068593-C-A

52499717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21068739-G-A

52499717-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21068739-G-C

52499789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21068803-C-T

52499845-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21068853-G-C

52499845-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21068853-G-T

52499875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21068880-C-T

http://identifiers.org/hco/6/GRCh38#52499915-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#21068920-C-A

52499919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21068924-T-C

52499932-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21068936-A-T

52499972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21068980-G-A

52499972-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21068980-G-T

52500031-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21069043-A-G

http://identifiers.org/hco/6/GRCh38#52500053-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#21069065-C-A

52500053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21069065-C-T

52500132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21069114-G-A

52500195-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21069175-A-G

52500196-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21069176-G-T

52500217-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21069197-A-T

52500367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21069348-C-T

52500477-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21069440-G-T

http://identifiers.org/hco/6/GRCh38#52500644-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#21069551-C-A

52500644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21069551-C-T

52500761-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21069660-T-C

52501014-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21069905-A-G

52501015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21069906-G-A

52501015-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21069906-G-C

52501015-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21069906-G-T

52501021-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21069911-A-G

52501061-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21069949-A-G

52501061-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21069949-A-T

52501191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21070040-G-A

52501191-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21070040-G-T

52501249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21070095-G-A

52501249-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21070095-G-T

52501299-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21070171-T-C

52501716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21070360-G-A

52501716-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21070360-G-T

52501884-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21070432-A-G

52501935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21070483-G-A

52501994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21070561-G-A

52502014-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21070580-T-C

52502097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21070655-C-T

http://identifiers.org/hco/6/GRCh38#52502106-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#21070664-A-C

52502597-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21071081-T-C

52502619-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21071083-T-C

52502794-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21071262-T-C

http://identifiers.org/hco/6/GRCh38#52502796-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#21071264-C-A

52502888-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21071350-A-G

52502888-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21071350-A-T

http://identifiers.org/hco/6/GRCh38#52502906-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#21071525-A-C

52502906-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21071525-A-G

52502973-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21071593-G-C

52502973-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21071593-G-T

52502974-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21071594-A-G

52503409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21071993-G-A

52503409-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21071993-G-C

http://identifiers.org/hco/6/GRCh38#52503437-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#21072011-C-A

http://identifiers.org/hco/6/GRCh38#52503608-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#21072172-C-A

52503608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21072172-C-T

http://identifiers.org/hco/6/GRCh38#52503609-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#21072173-C-A

52503609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21072173-C-T

http://identifiers.org/hco/6/GRCh38#52503642-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#21072205-C-A

52503777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 21072350-C-T

52503825-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21072399-T-C

52503961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21072615-C-T

52504013-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21072667-A-G

52504245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21072905-C-T

http://identifiers.org/hco/6/GRCh38#52504396-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#21073016-A-C

http://identifiers.org/hco/6/GRCh38#52504415-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#21073035-C-A

http://identifiers.org/hco/6/GRCh38#52504446-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#21073060-C-A

52504446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21073060-C-T

52504474-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21073091-G-C

52504474-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21073091-G-T

http://identifiers.org/hco/6/GRCh38#52504478-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#21073095-A-C

52504535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21073143-C-T

52504558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21073160-G-A

52504619-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 21073222-T-C

52504620-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 21073223-A-G

52504629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 21073232-G-A

52504629-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 21073232-G-T

52504644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 21073247-C-T

52504658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 21073261-C-T

52504669-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 21073272-A-T

52504700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 21073303-G-A

52504785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21073387-G-A

52504785-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21073387-G-T

http://identifiers.org/hco/6/GRCh38#52504803-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#21073405-C-A

52504886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21073454-C-T

52505341-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21073808-C-T

52505367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21073834-G-A

52505381-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21073854-G-T

52505478-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21073933-T-G

52505495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21073951-T-C

52505527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21073971-G-A

http://identifiers.org/hco/6/GRCh38#52505530-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#21073974-C-A

52505535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21073979-G-A

52505581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21074045-G-A

http://identifiers.org/hco/6/GRCh38#52505807-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#21074269-C-A

http://identifiers.org/hco/6/GRCh38#52505893-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#21074338-C-A

52505893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21074338-C-T

52505967-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21074376-T-A

http://identifiers.org/hco/6/GRCh38#52505973-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#21074382-C-A

52506016-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21074434-C-G

52506016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21074434-C-T

52506040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 21074458-G-A

52506040-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 21074458-G-C

52506043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 21074461-G-A

52506043-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 21074461-G-C

52506263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21074659-G-A

52506263-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21074659-G-T

http://identifiers.org/hco/6/GRCh38#52506268-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#21074664-C-A

52506268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21074664-C-T

52506383-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21074761-C-G

52506660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21074987-C-T

52506700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21075027-G-A

52506714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21075036-C-T

52506770-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21075058-A-G

52506787-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21075076-T-C

52506826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21075118-G-A

52506845-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21075137-T-C

52507036-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21075303-A-G

52507094-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21075358-G-A

52507094-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21075358-G-T

http://identifiers.org/hco/6/GRCh38#52507443-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#21075678-C-A

52507443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21075678-C-T

52507543-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21075781-T-C

52507543-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21075781-T-G

http://identifiers.org/hco/6/GRCh38#52507745-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#21075976-C-A

52507745-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21075976-C-G

52507749-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21075980-T-A

52507749-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21075980-T-G

http://identifiers.org/hco/6/GRCh38#52507755-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#21075986-A-C

52507921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21076122-C-T

52508003-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21076186-C-G

52508138-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21076277-T-A

52508138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21076277-T-C

52508145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21076284-G-A

52508145-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21076284-G-T

52508149-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21076288-A-G

52508164-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21076303-A-G

52508172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21076311-G-A

52508172-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21076311-G-C

52508172-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21076311-G-T

52508267-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 21076407-T-C

52508425-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21076549-G-T

52509155-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21076814-A-G

52509233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21076895-G-A

52509291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21076932-C-T

52509380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21077006-C-T

52509394-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21077012-A-G

52509404-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21077022-G-T

52509592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 21077141-G-A

52509644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21077193-C-T

52509659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21077206-G-A

52509659-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21077206-G-T

52509671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21077218-G-A

http://identifiers.org/hco/6/GRCh38#52509706-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#21077233-C-A

52509706-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21077233-C-G

52509706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21077233-C-T

http://identifiers.org/hco/6/GRCh38#52509848-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#21077352-C-A

52509848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21077352-C-T

52511414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21078224-C-T

52511637-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21078435-G-C

52511705-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21078460-T-A

http://identifiers.org/hco/6/GRCh38#52511849-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#21078611-C-A

52511849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21078611-C-T

52511930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21078697-G-A

52511945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21078719-G-A

52511945-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21078719-G-C

http://identifiers.org/hco/6/GRCh38#52512050-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#21078810-A-C

52512096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21078882-G-A

52512206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21079028-C-T

52512465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21079270-C-T

52512649-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21079471-T-C

52512752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21079563-C-T

52512807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21079619-T-C

52512978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21079815-T-C

52512992-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21079832-G-T

52513312-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21080182-T-C

52513383-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21080458-A-G

52513739-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21080783-G-C

52513850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21080901-G-A

52513957-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21080997-T-A

52514137-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21081120-G-C

http://identifiers.org/hco/6/GRCh38#52514180-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#21081163-A-C

52514232-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21081208-A-T

52514234-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21081210-T-C

52514258-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21081234-T-C

52514316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21081285-C-T

52514333-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21081302-G-C

52514345-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21081313-C-G

52514607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21081445-C-T

52514662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21081475-G-A

52514662-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21081475-G-C

52514730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21081558-G-A

52514864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21081677-G-A

52515101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21081917-C-T

52515147-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21081953-T-C

52515156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21081961-G-A

52515257-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21082025-G-C

52515319-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21082080-A-G

52515600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21082611-C-T

52515618-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21082629-G-C

http://identifiers.org/hco/6/GRCh38#52515761-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#21082812-C-A

52515761-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21082812-C-G

52515773-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21082823-G-C

http://identifiers.org/hco/6/GRCh38#52515787-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#21082837-C-A

52515800-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21082842-T-C

http://identifiers.org/hco/6/GRCh38#52515811-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#21082853-C-A

http://identifiers.org/hco/6/GRCh38#52515839-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#21082890-A-C

52515839-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21082890-A-T

52515840-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21082891-T-A

52515840-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21082891-T-C

52515921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 21082946-T-C

52515929-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 21082954-T-G

52515931-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant, stop_lost
orthologous variants: 21082956-T-A

52515953-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21082972-A-G

52515957-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21082976-G-T

52515974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21082985-C-T

52515977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21082988-C-T

52515978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21082989-C-T

52515985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21082996-G-A

52515992-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21083003-T-C

52515992-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21083003-T-G

52516011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 21083022-C-T

52516039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 21083050-G-A

52516141-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21083152-C-G

52516141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21083152-C-T

http://identifiers.org/hco/6/GRCh38#52516220-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#21083225-C-A

52516220-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21083225-C-G

52516220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21083225-C-T

52516326-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21083316-A-G

52516328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21083318-G-A

http://identifiers.org/hco/6/GRCh38#52516368-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#21083357-A-C

52516387-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21083378-A-G

http://identifiers.org/hco/6/GRCh38#52516394-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#21083385-C-A

52516394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21083385-C-T

52516406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21083406-G-A

52516406-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21083406-G-T

52516422-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21083427-A-G

52516423-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21083428-T-G

52516426-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21083431-A-T

http://identifiers.org/hco/6/GRCh38#52516429-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#21083434-C-A

52516429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21083434-C-T

52516516-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21083497-A-G

52516555-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21083536-C-G

52516555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21083536-C-T

52516570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21083552-C-T

52516573-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21083555-C-G

52516573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21083555-C-T

52516577-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21083559-C-G

52516577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21083559-C-T

http://identifiers.org/hco/6/GRCh38#52516580-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#21083562-A-C

52516818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21083814-G-A

52516818-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21083814-G-T

http://identifiers.org/hco/6/GRCh38#52516842-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#21083838-C-A

52516842-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21083838-C-G

52516863-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21083857-T-C

http://identifiers.org/hco/6/GRCh38#52516883-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#21083877-C-A

52516883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21083877-C-T

52516903-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21083897-G-T

http://identifiers.org/hco/6/GRCh38#52516913-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#21083907-C-A

52517100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21084096-T-C

http://identifiers.org/hco/6/GRCh38#52517113-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#21084109-C-A

http://identifiers.org/hco/6/GRCh38#52517126-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#21084121-A-C

http://identifiers.org/hco/6/GRCh38#52517378-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#21084516-C-A

52517581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21084765-G-A

52518169-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21085299-A-G

52518432-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21085526-T-C

52523212-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21095769-T-G

52523281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21095838-G-A

52523281-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21095838-G-T

52523283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21095840-G-A

52523283-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21095840-G-T

http://identifiers.org/hco/6/GRCh38#52524932-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#21098284-C-A

52524932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21098284-C-T

52525109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21098474-G-A

52525109-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21098474-G-T

http://identifiers.org/hco/6/GRCh38#52525171-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#21098517-C-A

52525452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21098818-C-T

http://identifiers.org/hco/6/GRCh38#52525472-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#21098839-C-A

52525473-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21098840-A-T

52525906-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21099021-T-C

52525956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21099055-G-A

52525956-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21099055-G-C

http://identifiers.org/hco/6/GRCh38#52525974-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#21099066-A-C

52526209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21099225-G-A

52526209-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21099225-G-T

52526258-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21099274-C-G

52526258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21099274-C-T

52526261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21099277-A-G

52526866-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21099576-T-C

http://identifiers.org/hco/6/GRCh38#52526932-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#21099691-A-C

52529407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21100641-G-A

52529407-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21100641-G-T

http://identifiers.org/hco/6/GRCh38#52529408-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#21100642-A-C

52529409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21100643-G-A

52529409-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21100643-G-T

52529853-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21101175-G-T

http://identifiers.org/hco/6/GRCh38#52529886-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16406
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#21101222-C-A