28138380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 147367176-G-A

28138380-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 147367176-G-T

http://identifiers.org/hco/13/GRCh38#28138530-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147367287-C-A

28138530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 147367287-C-T

28138654-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 147367386-T-C

28138654-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 147367386-T-G

http://identifiers.org/hco/13/GRCh38#28138672-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147367404-C-A

28138672-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 147367404-C-G

28138672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 147367404-C-T

http://identifiers.org/hco/13/GRCh38#28138684-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147367422-C-A

28138684-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 147367422-C-G

28138684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 147367422-C-T

http://identifiers.org/hco/13/GRCh38#28138711-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147367449-C-A

28138711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 147367449-C-T

http://identifiers.org/hco/13/GRCh38#28138894-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147367644-C-A

28138894-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 147367644-C-G

28138894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 147367644-C-T

28138957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 147367707-G-A

28138957-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 147367707-G-T

http://identifiers.org/hco/13/GRCh38#28139059-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147367791-C-A

28139059-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 147367791-C-G

28139059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 147367791-C-T

28139302-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147368014-G-C

28139318-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147368030-G-T

28139335-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147368061-T-G

28139340-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147368066-T-G

28139472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147368186-C-T

28139576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147368269-C-T

28139582-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147368275-G-T

28139700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147368366-T-C

28139753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147368420-C-T

28140445-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147368702-G-T

http://identifiers.org/hco/13/GRCh38#28143271-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147374588-C-A

28143296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147374613-G-A

28143458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147374761-A-G

28147124-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-G

28147169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-A

28147210-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-C

28169554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147382487-G-A

28169614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147382542-T-C

28171294-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147383791-A-G

28173714-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147386728-T-A

28174261-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147387452-T-G

http://identifiers.org/hco/13/GRCh38#28174305-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147387496-C-A

28174305-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 147387496-C-G

28174305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 147387496-C-T

28174525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147387676-G-A

28174767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147387826-C-T

28174944-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147387993-T-C

28174968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147388017-A-G

28175892-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147389484-A-G

28176339-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147389866-A-T

28176407-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147389976-A-G

http://identifiers.org/hco/13/GRCh38#28176611-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147390168-C-A

28176611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147390168-C-T

28176870-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147391048-A-T

28177073-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147391224-T-A

28177073-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147391224-T-C

28177619-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147391671-G-C

28177643-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147391694-A-G

http://identifiers.org/hco/13/GRCh38#28177792-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147391860-C-A

28177792-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147391860-C-G

28177839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147391902-G-A

28178520-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147393216-A-T

28178641-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147393319-A-T

28179009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147393571-A-G

28179080-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147393640-C-G

28179080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147393640-C-T

28179326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147393855-C-T

28179387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147393914-G-A

28179757-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147393987-G-T

28180110-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147394609-T-G

28180325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147394773-G-A

28180535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147394845-C-T

28180897-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147395051-A-G

http://identifiers.org/hco/13/GRCh38#28181117-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147395221-A-C

28181169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147395263-G-A

28181246-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147395332-T-C

28181766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147395762-C-T

28181868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147395877-G-A

28181882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147395898-T-C

28182387-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147396344-A-G

28182635-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147396518-A-G

28182710-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147396583-C-G

28182774-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147396642-T-C

28185543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147396983-G-A

28185582-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147397020-G-C

http://identifiers.org/hco/13/GRCh38#28186270-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147397659-C-A

28188844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147398820-A-G

28192635-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147400655-T-C

28192792-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147400799-T-A

28192876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147400901-G-A

28194981-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147402129-T-C

28196185-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147402748-T-G

28197039-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147403617-G-T

28197078-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147403650-G-A

28197263-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 147403824-A-G

28197298-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 147403859-A-G

28197302-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 147403863-A-G

28197306-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 147403867-A-G

28197311-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 147403872-G-C

28197513-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147404071-T-A

28197513-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147404071-T-G

28198655-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147404775-T-C

28198941-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147404992-T-C

28199032-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147405080-T-G

http://identifiers.org/hco/13/GRCh38#28199474-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147405611-C-A

28199474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147405611-C-T

28199563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147405686-C-T

28199624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147405739-T-C

28199624-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147405739-T-G

28199676-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147405837-T-A

28200102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147406258-C-T

28205144-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147411460-T-C

28205224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147411539-G-A

28206116-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147411960-C-G

28206129-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147411973-A-G

28206129-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147411973-A-T

28207217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147414185-G-A

28207217-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147414185-G-T

http://identifiers.org/hco/13/GRCh38#28207234-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147414200-A-C

28207234-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147414200-A-T

28207350-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147414295-G-T

28207528-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147414452-A-G

28207716-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147414612-C-G

28207900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147414766-A-G

28207926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147414782-C-T

28207927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147414783-G-A

28208131-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147414907-T-C

28208249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147415021-G-A

28208467-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147415201-T-G

28208816-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147415290-A-G

http://identifiers.org/hco/13/GRCh38#28218415-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147422744-C-A

28218442-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147422766-G-T

28219521-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147424290-A-G

http://identifiers.org/hco/13/GRCh38#28219572-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147424329-A-C

28219740-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147424482-A-G

http://identifiers.org/hco/13/GRCh38#28219856-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147424573-C-A

28219856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147424573-C-T

28220095-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147424791-G-T

http://identifiers.org/hco/13/GRCh38#28220107-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147424803-C-A

28221725-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147425372-T-C

28221763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147425398-C-T

28221828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147425434-C-T

28222115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147425680-C-T

28222219-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147425836-A-G

28223410-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147426555-T-C

28223459-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147426595-T-C

http://identifiers.org/hco/13/GRCh38#28223686-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147426699-A-C

28223755-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147426761-A-G

28225220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147427564-G-A

28225371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147427691-G-A

28225371-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147427691-G-C

28225497-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147427801-G-C

28225713-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147428001-A-G

http://identifiers.org/hco/13/GRCh38#28226324-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147428499-C-A

28226324-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147428499-C-G

28226584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147428722-G-A

28226584-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147428722-G-C

28226584-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147428722-G-T

28226602-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147428737-A-G

28226835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147428967-T-C

28228108-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147430152-A-G

28228347-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147430397-T-A

28229023-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147430840-T-G

28229035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147430854-G-A

28229163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147430952-C-T

28231216-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147431641-A-G

28231245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147431666-A-G

28231325-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147431725-T-C

28231911-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147432310-A-G

28237298-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147437670-A-T

28237379-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147437730-A-G

28237491-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147437819-T-C

28237535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147437845-G-A

28237535-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147437845-G-T

28237610-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147437912-T-G

28237659-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147437952-A-T

http://identifiers.org/hco/13/GRCh38#28238376-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147438625-A-C

28238508-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147438731-A-G

28238801-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147439183-T-C

28238856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147439253-G-A

http://identifiers.org/hco/13/GRCh38#28239146-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147439511-A-C

28239146-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147439511-A-G

28239146-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147439511-A-T

28239283-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147439564-T-C

28239521-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147439837-G-T

http://identifiers.org/hco/13/GRCh38#28239753-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147440069-C-A

28239753-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 147440069-C-G

28239753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 147440069-C-T

http://identifiers.org/hco/13/GRCh38#28240002-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147440297-A-C

28245335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147447318-G-A

28245408-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147447375-G-T

28245848-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147447741-A-G

28245891-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147447760-A-G

28246033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147447904-G-A

http://identifiers.org/hco/13/GRCh38#28246050-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147447921-C-A

28246094-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147448001-G-C

28253274-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147453615-T-C

28253521-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147453806-C-G

28254303-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147454524-A-G

http://identifiers.org/hco/13/GRCh38#28254532-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147454732-C-A

http://identifiers.org/hco/13/GRCh38#28254648-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147454839-A-C

28254697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147454890-G-A

28254720-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147454908-T-C

28255333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147455503-G-A

28255333-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147455503-G-T

28255727-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147455834-A-G

http://identifiers.org/hco/13/GRCh38#28255729-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147455836-C-A

28255729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147455836-C-T

28255758-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147455868-G-T

28255974-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147456036-T-G

28256263-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147456286-A-G

28256420-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 147456443-A-G

http://identifiers.org/hco/13/GRCh38#28256621-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147456643-C-A

28256647-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147456685-T-A

28256647-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147456685-T-C

28256758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147456751-A-G

28257030-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147457019-A-G

28260479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 147458672-T-C

28260479-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 147458672-T-G

28260539-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 147458732-T-C

28260574-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147458765-A-G

28260576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147458767-G-A

28260576-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147458767-G-T

28260593-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147458784-T-A

28260593-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147458784-T-C

28260603-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147458794-T-A

28260618-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147458805-A-G

28260637-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147458816-A-G

http://identifiers.org/hco/13/GRCh38#28260652-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147458831-A-C

http://identifiers.org/hco/13/GRCh38#28260673-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147458848-C-A

28260673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147458848-C-T

28260674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147458849-G-A

28261019-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147459355-A-G

28261142-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147459624-G-T

28261165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147459694-C-T

28261474-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147460059-A-G

http://identifiers.org/hco/13/GRCh38#28266379-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147463034-A-C

28266455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147463093-G-A

28266612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147463226-G-A

28266612-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147463226-G-T

28266627-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147463241-T-C

http://identifiers.org/hco/13/GRCh38#28266747-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147463361-C-A

28266747-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 147463361-C-G

28266747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 147463361-C-T

http://identifiers.org/hco/13/GRCh38#28266944-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147463553-A-C

28266944-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147463553-A-T

28266959-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147463572-A-G

http://identifiers.org/hco/13/GRCh38#28267014-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147463674-A-C

28267014-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147463674-A-G

28267201-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 147463841-T-G

28267488-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147464121-T-A

28267962-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147464211-A-G

28268573-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147464557-A-G

28268657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 147464637-G-A

http://identifiers.org/hco/13/GRCh38#28268780-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147464676-C-A

28268870-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 147464761-A-T

28269036-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 147464926-G-C

28269065-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 147464956-T-C

28269359-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147465206-A-G

28269359-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147465206-A-T

28269692-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147465893-T-G

28269866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147466085-A-G

28270067-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147466312-A-G

28270085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147466330-A-G

28271338-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147467374-C-T

http://identifiers.org/hco/13/GRCh38#28271406-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147467452-A-C

28271418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147467464-G-A

28271640-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147467699-T-G

28271660-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147467723-C-G

28271770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147467866-T-C

28271784-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147467880-A-G

28272005-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 147468051-T-C

http://identifiers.org/hco/13/GRCh38#28273946-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147468927-A-C

28274211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147469158-G-A

28274221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147469168-C-T

28274509-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147469533-A-G

28274511-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147469535-T-A

28274511-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147469535-T-G

28274663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147469779-G-A

28274770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147469886-G-A

28274779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147469895-G-A

28274781-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147469897-G-C

28275126-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147470247-A-G

28275155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147470279-G-A

28275155-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147470279-G-T

28275421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 147470489-C-T

http://identifiers.org/hco/13/GRCh38#28275826-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147470832-A-C

28275888-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 147470902-T-C

28275957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 147470967-G-A

28276529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 147472337-G-A

28276716-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 147472501-C-G

28276760-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 147472537-A-G

http://identifiers.org/hco/13/GRCh38#28277445-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147473401-A-C

28277445-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron variant
orthologous variants: 147473401-A-G

28277445-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron variant
orthologous variants: 147473401-A-T

28277705-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron variant
orthologous variants: 147473596-T-C

28277804-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron variant
orthologous variants: 147473697-A-T

http://identifiers.org/hco/13/GRCh38#28277997-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147473843-C-A

28278508-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron variant
orthologous variants: 147474377-G-T

28278615-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron variant
orthologous variants: 147474492-A-G

28278831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron variant
orthologous variants: 147474705-G-A

http://identifiers.org/hco/13/GRCh38#28278998-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147475247-A-C

28281169-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147476410-T-A

28281200-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147476440-A-T

28281254-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147476493-T-A

28281254-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147476493-T-C

28281733-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147476923-T-G

28282152-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147477015-C-G

28282237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147477087-C-T

28287765-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 147479685-G-C

28287932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 147479830-G-A

28288180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron variant
orthologous variants: 147480320-G-A

28288180-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron variant
orthologous variants: 147480320-G-T

28288186-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron variant
orthologous variants: 147480326-T-G

http://identifiers.org/hco/13/GRCh38#28288225-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147480365-C-A

28288225-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron variant
orthologous variants: 147480365-C-G

28291192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron variant
orthologous variants: 147481579-G-A

28291415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron variant
orthologous variants: 147481745-A-G

28291557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron variant
orthologous variants: 147481775-C-T

28291571-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron variant
orthologous variants: 147481789-T-G

28291591-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron variant
orthologous variants: 147481808-A-T

28291612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron variant
orthologous variants: 147481835-C-T

28291890-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron variant
orthologous variants: 147482007-T-G

28292339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron variant
orthologous variants: 147482371-C-T

28292349-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron variant
orthologous variants: 147482381-T-C

http://identifiers.org/hco/13/GRCh38#28292357-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147482389-A-C

28292368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron variant
orthologous variants: 147482400-A-G

28292370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: intron variant
orthologous variants: 147482402-A-G

28292617-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: 3 prime UTR variant
orthologous variants: 147482650-G-T

28292670-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: 3 prime UTR variant
orthologous variants: 147482706-T-A

28292670-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: 3 prime UTR variant
orthologous variants: 147482706-T-C

28292700-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: 3 prime UTR variant
orthologous variants: 147482735-A-G

28292700-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: 3 prime UTR variant
orthologous variants: 147482735-A-T

28292735-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: 3 prime UTR variant
orthologous variants: 147482761-G-T

28292743-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: 3 prime UTR variant
orthologous variants: 147482769-T-A

28292754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: 3 prime UTR variant
orthologous variants: 147482779-T-C

28292867-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: 3 prime UTR variant
orthologous variants: 147482891-T-A

28292867-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: 3 prime UTR variant
orthologous variants: 147482891-T-C

28292867-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: 3 prime UTR variant
orthologous variants: 147482891-T-G

28292873-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: 3 prime UTR variant
orthologous variants: 147482897-T-A

28292873-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: 3 prime UTR variant
orthologous variants: 147482897-T-C

28292938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: 3 prime UTR variant
orthologous variants: 147482958-T-C

28292993-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: 3 prime UTR variant
orthologous variants: 147482994-T-A

28292996-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: 3 prime UTR variant
orthologous variants: 147482997-A-G

28293018-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: 3 prime UTR variant
orthologous variants: 147483019-T-G

28293024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: 3 prime UTR variant
orthologous variants: 147483025-G-A

28293024-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: 3 prime UTR variant
orthologous variants: 147483025-G-C

28293024-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: 3 prime UTR variant
orthologous variants: 147483025-G-T

28293110-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: 3 prime UTR variant
orthologous variants: 147483100-T-G

28293149-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: 3 prime UTR variant
orthologous variants: 147483140-T-C

http://identifiers.org/hco/13/GRCh38#28293155-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147483146-C-A

28293155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: 3 prime UTR variant
orthologous variants: 147483146-C-T

28293394-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: 3 prime UTR variant
orthologous variants: 147483375-T-G

28293400-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: 3 prime UTR variant
orthologous variants: 147483381-T-G

28294710-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29991
most severe consequence: 3 prime UTR variant
orthologous variants: 147484628-A-G