53708949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 102613362-G-A

53709017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 102613438-G-A

53709121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 102613525-T-C

http://identifiers.org/hco/12/GRCh38#53709138-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#102613533-C-A

53709175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 102613567-G-A

53709175-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 102613567-G-T

http://identifiers.org/hco/12/GRCh38#53709176-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#102613568-C-A

53709176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 102613568-C-T

53709221-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 102613614-A-G

53709278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 102613667-T-C

53709461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 102613747-A-G

53709472-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 102613758-A-G

53709487-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 102613773-T-A

53709487-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 102613773-T-C

http://identifiers.org/hco/12/GRCh38#53709493-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#102613779-C-A

53709493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 102613779-C-T

53709543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 102613831-G-A

53709543-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 102613831-G-T

53709546-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 102613834-G-C

53709546-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 102613834-G-T

53709557-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 102613844-G-T

http://identifiers.org/hco/12/GRCh38#53709572-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#102613859-C-A

53709572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 102613859-C-T

53709643-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 102613922-A-G

53709679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 102613958-T-C

53709698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 102613964-G-A

53710040-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 102614283-T-A

53710040-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 102614283-T-C

53710291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 102614538-G-A

53710291-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 102614538-G-C

53710291-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 102614538-G-T

53710326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 102614580-G-A

53710326-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 102614580-G-T

http://identifiers.org/hco/12/GRCh38#53710380-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#102614628-C-A

53710380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 102614628-C-T

53710385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 102614633-G-A

53710385-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 102614633-G-T

53710395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 102614643-G-A

53710395-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 102614643-G-T

53710399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 102614647-G-A

53710399-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 102614647-G-T

53710400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 102614648-A-G

53710400-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 102614648-A-T

53710402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 102614650-G-A

53710402-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 102614650-G-T

53710625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 102614863-C-T

53710688-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 102614882-A-G

53710712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 102614905-C-T

53710726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 102614919-C-T

http://identifiers.org/hco/12/GRCh38#53710916-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#102615034-C-A

53710916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 102615034-C-T

http://identifiers.org/hco/12/GRCh38#53710917-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#102615035-A-C

53710917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 102615035-A-G

53710919-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 102615057-A-G

http://identifiers.org/hco/12/GRCh38#53710923-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#102615061-C-A

53710923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 102615061-C-T

http://identifiers.org/hco/12/GRCh38#53710926-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#102615064-C-A

53711073-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 102615170-T-C

53711159-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 102615259-G-C

53711159-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 102615259-G-T

http://identifiers.org/hco/12/GRCh38#53711213-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#102615321-C-A

53711213-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 102615321-C-G

53711213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 102615321-C-T

http://identifiers.org/hco/12/GRCh38#53711214-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#102615322-C-A

http://identifiers.org/hco/12/GRCh38#53711697-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#102615554-C-A

53711697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 102615554-C-T

53711826-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 102615677-G-T

http://identifiers.org/hco/12/GRCh38#53712076-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#102615936-A-C

53712197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 102616182-G-A

53712204-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 102616189-T-A

53712204-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 102616189-T-C

53712214-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 102616194-T-A

53712214-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 102616194-T-G

http://identifiers.org/hco/12/GRCh38#53712250-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#102616237-C-A

http://identifiers.org/hco/12/GRCh38#53712276-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#102616262-C-A

53712276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 102616262-C-T

53712322-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 102616295-T-C

53712678-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 102616638-G-C

53712678-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 102616638-G-T

http://identifiers.org/hco/12/GRCh38#53712701-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#102616663-C-A

53712755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 102616697-G-A

53712755-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 102616697-G-T

53712781-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 102616722-G-T

http://identifiers.org/hco/12/GRCh38#53712789-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#102616730-A-C

53712789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 102616730-A-G

53713012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 102616922-G-A

53713012-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 102616922-G-T

http://identifiers.org/hco/12/GRCh38#53713018-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#102616927-A-C

http://identifiers.org/hco/12/GRCh38#53713022-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#102616931-C-A

53713022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 102616931-C-T

53713024-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 102616933-T-C

53713171-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 102617052-A-G

53713192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 102617073-C-T

53713216-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102617092-A-G

53713216-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102617092-A-T

53713226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102617102-G-A

53713353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102617216-G-A

53713353-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102617216-G-T

http://identifiers.org/hco/12/GRCh38#53713636-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#102617460-C-A

53713716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 102617526-G-A

http://identifiers.org/hco/12/GRCh38#53713719-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#102617529-C-A

53713719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 102617529-C-T

http://identifiers.org/hco/12/GRCh38#53713728-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#102617538-C-A

53713728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 102617538-C-T

53713758-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 102617568-C-G

53713758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 102617568-C-T

http://identifiers.org/hco/12/GRCh38#53713785-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#102617595-C-A

53713827-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 102617637-A-G

53713827-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 102617637-A-T

53713884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 102617694-C-T

53713978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102617766-G-A

53713978-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102617766-G-T

http://identifiers.org/hco/12/GRCh38#53713991-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#102617779-C-A

53714013-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102617801-G-T

53714090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102617837-G-A

53714090-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102617837-G-T

53714091-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102617838-T-A

53714091-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102617838-T-C

http://identifiers.org/hco/12/GRCh38#53714092-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#102617839-A-C

53714106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102617853-G-A

53714106-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102617853-G-T

53714155-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 102617900-A-G

53714176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 102617921-A-G

53714277-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102618021-A-G

53714286-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102618028-T-C

53714287-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102618029-G-T

53714379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102618074-G-A

53714379-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102618074-G-T

53714398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102618093-C-T

53714495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102618196-G-A

53714495-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102618196-G-T

53714522-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102618224-G-T

53714607-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 102618315-C-G

53714607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 102618315-C-T

53714705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102618413-G-A

53714705-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102618413-G-C

53714705-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102618413-G-T

http://identifiers.org/hco/12/GRCh38#53714809-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#102618515-C-A

53714809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102618515-C-T

53714811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102618517-G-A

53714811-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102618517-G-T

http://identifiers.org/hco/12/GRCh38#53714841-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#102618541-C-A

53714841-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102618541-C-G

53714845-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102618545-T-C

http://identifiers.org/hco/12/GRCh38#53715020-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#102618696-C-A

53715020-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102618696-C-T

53715252-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 102618892-G-T

http://identifiers.org/hco/12/GRCh38#53715343-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#102618980-A-C

http://identifiers.org/hco/12/GRCh38#53715451-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#102619091-C-A

53715451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102619091-C-T

53715534-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102619129-T-C

53715605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102619209-A-G

53715606-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102619210-T-A

53715606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102619210-T-C

53715755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102619335-G-A

53715755-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102619335-G-C

http://identifiers.org/hco/12/GRCh38#53715879-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#102619435-C-A

53715879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 102619435-C-T

53716095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102619645-C-T

53716116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102619658-C-T

53716147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102619671-G-A

53716147-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102619671-G-T

53716226-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102619743-T-C

53716226-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102619743-T-G

53716323-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 102619841-A-G

53716344-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 102619862-T-C

53716364-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 102619882-T-G

53716410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 102619928-C-T

53716453-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102619971-T-C

53716459-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102619977-G-C

53716512-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102620075-T-A

53716533-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102620096-G-T

53716791-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102620408-A-T

53717608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102621141-G-A

53719708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102622260-G-A

53719712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102622264-A-G

http://identifiers.org/hco/12/GRCh38#53719778-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#102622330-C-A

53719778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 102622330-C-T

53719864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102622402-C-T

53720050-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102622632-T-C

53720467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102622930-G-A

53720467-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102622930-G-C

53720919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102623251-T-C

53721070-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102623576-T-A

53721179-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102623827-T-A

53721179-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102623827-T-C

53721181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102623829-C-T

53721290-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102623986-A-G

53721345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102624041-G-A

53721345-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102624041-G-T

53721354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102624050-G-A

53721354-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102624050-G-T

53721447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102624140-G-A

53721686-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102624373-A-G

http://identifiers.org/hco/12/GRCh38#53721734-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#102624413-C-A

53721734-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102624413-C-G

53721734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102624413-C-T

53721765-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102624439-T-C

53721765-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102624439-T-G

53721880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102624544-G-A

53721880-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102624544-G-T

53721903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102624566-C-T

http://identifiers.org/hco/12/GRCh38#53721944-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#102624608-C-A

53721944-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102624608-C-G

53721944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102624608-C-T

53722004-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102624644-C-G

53722004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102624644-C-T

53722418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102625026-C-T

53723175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102626033-G-A

53723565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102626206-G-A

53723835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102626482-C-T

http://identifiers.org/hco/12/GRCh38#53723841-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#102626488-C-A

53723841-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102626488-C-G

53723882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102626542-C-T

http://identifiers.org/hco/12/GRCh38#53723944-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#102626602-A-C

53723944-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102626602-A-G

http://identifiers.org/hco/12/GRCh38#53723948-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#102626606-C-A

53723948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102626606-C-T

53723949-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102626607-A-G

53723954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102626612-C-T

53723999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102626659-C-T

53724031-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102626706-T-C

http://identifiers.org/hco/12/GRCh38#53724063-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#102626750-C-A

53724063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102626750-C-T

53724600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102627333-C-T

http://identifiers.org/hco/12/GRCh38#53724601-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#102627334-A-C

53724750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 102627514-G-A

53724799-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102627550-G-T

53724875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102627801-G-A

53724947-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102627858-A-G

53724947-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102627858-A-T

53725282-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102628172-T-A

53725282-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102628172-T-C

http://identifiers.org/hco/12/GRCh38#53725290-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#102628180-C-A

53725290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102628180-C-T

http://identifiers.org/hco/12/GRCh38#53725297-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#102628185-C-A

http://identifiers.org/hco/12/GRCh38#53725318-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#102628204-C-A

http://identifiers.org/hco/12/GRCh38#53725334-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#102628217-C-A

53725334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102628217-C-T

http://identifiers.org/hco/12/GRCh38#53725335-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#102628218-C-A

53725335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102628218-C-T

http://identifiers.org/hco/12/GRCh38#53725349-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#102628232-C-A

53725349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102628232-C-T

http://identifiers.org/hco/12/GRCh38#53725360-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#102628243-C-A

53725360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102628243-C-T

53725390-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102628255-G-T

53725570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102628418-G-A

53725570-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102628418-G-T

http://identifiers.org/hco/12/GRCh38#53725617-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#102628454-C-A

53725617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102628454-C-T

53725635-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102628525-G-C

53725651-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102628541-T-A

53725651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102628541-T-C

53725684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102628576-C-T

53725796-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102628645-G-T

53725807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102628656-G-A

http://identifiers.org/hco/12/GRCh38#53725825-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#102628674-A-C

http://identifiers.org/hco/12/GRCh38#53725863-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#102628716-C-A

53726053-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102628907-G-T

53726093-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102628947-A-G

53726149-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102629005-A-G

53726182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102629035-G-A

53726182-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102629035-G-C

http://identifiers.org/hco/12/GRCh38#53726208-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#102629064-C-A

53726208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 102629064-C-T

http://identifiers.org/hco/12/GRCh38#53726224-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#102629080-C-A

53726224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 102629080-C-T

http://identifiers.org/hco/12/GRCh38#53726265-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#102629136-C-A

53726328-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 102629215-A-G

53726328-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 102629215-A-T

53726459-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 102629577-C-G

53726463-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 102629581-G-T

53726760-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 102629845-T-A

53726950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 102630035-G-A

53726953-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 102630038-G-T

53727304-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 102630384-T-A

53727304-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 102630384-T-C

53727532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 102630605-C-T

53727719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 102630793-G-A

53727719-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 102630793-G-T

53727731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 102630805-G-A

53727731-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29306
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 102630805-G-T