212950522-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 190711481-T-C

http://identifiers.org/hco/1/GRCh38#212950561-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#190711442-C-A

212950561-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 190711442-C-G

212950561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 190711442-C-T

212950802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190711282-C-T

212951025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 190711046-G-A

212951054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190711019-C-T

http://identifiers.org/hco/1/GRCh38#212951077-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190710997-A-C

212951212-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 190710870-T-G

http://identifiers.org/hco/1/GRCh38#212951216-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190710866-C-A

212951218-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 190710864-G-T

http://identifiers.org/hco/1/GRCh38#212951299-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190710820-C-A

http://identifiers.org/hco/1/GRCh38#212951400-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190710748-C-A

http://identifiers.org/hco/1/GRCh38#212951449-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190710697-C-A

212951449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 190710697-C-T

http://identifiers.org/hco/1/GRCh38#212951563-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190710631-C-A

212951563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 190710631-C-T

212951862-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190710332-G-T

212951922-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190710275-G-C

212951922-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190710275-G-T

212952113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190710169-A-G

212952207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190710078-G-A

212952224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190710060-C-T

212952228-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190710056-G-T

http://identifiers.org/hco/1/GRCh38#212952442-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190709847-C-A

212952442-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 190709847-C-T

212952639-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 190709668-G-T

212952710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 190709628-G-A

212952712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 190709626-A-G

212952734-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 190709605-G-C

212952739-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 190709600-T-C

http://identifiers.org/hco/1/GRCh38#212952759-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190709581-C-A

212952789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 190709550-A-G

http://identifiers.org/hco/1/GRCh38#212952813-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190709532-C-A

212952813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190709532-C-T

212952859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190709483-C-T

212953105-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190709247-A-G

212953237-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190709139-G-C

212953237-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190709139-G-T

212955138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190707590-G-A

212955265-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190707473-A-G

212955408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190707350-G-A

212955541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190707231-G-A

http://identifiers.org/hco/1/GRCh38#212955684-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190707094-C-A

212955866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190706928-C-T

212955949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190706834-C-T

212956010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190706778-C-T

212957937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190705390-C-T

212958029-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190705302-A-G

212958130-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190705225-C-G

212958521-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190704912-G-T

212958657-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190704812-A-G

212958725-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190704774-T-C

212959411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190704314-C-T

http://identifiers.org/hco/1/GRCh38#212959687-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190704052-C-A

212959709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190704030-C-T

212959796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 190703966-G-A

212959851-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 190703933-T-C

212960541-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190703306-A-G

212960671-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190703201-T-C

http://identifiers.org/hco/1/GRCh38#212960704-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190703162-A-C

212960951-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190702883-C-G

http://identifiers.org/hco/1/GRCh38#212961014-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190702825-C-A

212961014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190702825-C-T

http://identifiers.org/hco/1/GRCh38#212961053-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190702795-C-A

212961053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190702795-C-T

212961293-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 190702561-G-T

212961294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 190702560-G-A

212961294-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 190702560-G-C

http://identifiers.org/hco/1/GRCh38#212961390-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190702466-C-A

http://identifiers.org/hco/1/GRCh38#212961434-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190702437-A-C

212961434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190702437-A-G

212961443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190702428-G-A

212961443-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190702428-G-T

http://identifiers.org/hco/1/GRCh38#212961461-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190702410-C-A

212961461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190702410-C-T

http://identifiers.org/hco/1/GRCh38#212961468-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190702390-C-A

212961468-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190702390-C-G

http://identifiers.org/hco/1/GRCh38#212961499-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190702352-C-A

212961499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190702352-C-T

212961518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190702344-C-T

212961526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190702340-C-T

212961543-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190702324-T-A

212961543-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190702324-T-G

212961607-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190702298-C-G

212961679-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190702275-T-G

212962069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190702145-G-A

212962130-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190702089-T-C

212962130-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190702089-T-G

http://identifiers.org/hco/1/GRCh38#212962261-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190701967-C-A

212962261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190701967-C-T

212962266-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190701962-G-C

212962331-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190701903-T-C

http://identifiers.org/hco/1/GRCh38#212962342-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190701888-A-C

212962342-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190701888-A-T

212962644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190701667-G-A

212962754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190701567-C-T

212962755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190701566-G-A

212962781-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190701544-G-T

212963036-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190701349-C-G

212963157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190701245-G-A

212963204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190701200-C-T

212963351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190701079-C-T

http://identifiers.org/hco/1/GRCh38#212963406-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190701044-C-A

212963407-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190701043-T-C

http://identifiers.org/hco/1/GRCh38#212963442-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190701018-A-C

212963442-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190701018-A-G

212963491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190700969-G-A

212964054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190700536-C-T

212964055-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190700535-A-G

212964088-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190700509-G-C

212964422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190700276-G-A

212964667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190700060-C-T

212964791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190699941-C-T

212964812-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190699920-C-G

212964820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190699912-T-C

212965427-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190699460-G-T

212965439-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190699448-G-C

212965468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190699419-C-T

212965577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190699310-C-T

212965590-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190699297-T-G

http://identifiers.org/hco/1/GRCh38#212965632-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190699263-C-A

212965632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190699263-C-T

212965653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190699242-A-G

http://identifiers.org/hco/1/GRCh38#212965666-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190699233-A-C

212965666-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190699233-A-G

212965696-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190699206-A-G

212965714-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 190699188-T-C

212965788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 190699114-G-A

212965788-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 190699114-G-T

212965791-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 190699111-T-C

212965791-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 190699111-T-G

http://identifiers.org/hco/1/GRCh38#212965815-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190699087-C-A

212965815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 190699087-C-T

212965908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 190699000-G-A

212965908-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 190699000-G-T

212965910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 190698998-G-A

212965910-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 190698998-G-T

http://identifiers.org/hco/1/GRCh38#212965919-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190698989-C-A

212965919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 190698989-C-T

212965994-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 190698910-G-T

212966074-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 190698693-G-T

212966098-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 190698670-T-C

212966098-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 190698670-T-G

212966106-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 190698661-T-A

http://identifiers.org/hco/1/GRCh38#212966108-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190698659-A-C

212966116-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 190698639-T-G

212966117-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 190698638-G-T

http://identifiers.org/hco/1/GRCh38#212966118-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190698637-C-A

212966118-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 190698637-C-G

212966122-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 190698633-G-T

212966199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190698548-G-A

212966203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190698544-G-A

212966203-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190698544-G-C

212966203-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190698544-G-T

212966222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190698521-T-C

212966361-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190698382-T-C

212966530-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190698267-T-A

212967067-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 190697886-G-T

212967073-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 190697873-T-C

212967076-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 190697870-A-G

212967080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 190697866-G-A

212967080-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 190697866-G-C

212967082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 190697864-C-T

http://identifiers.org/hco/1/GRCh38#212967099-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190697847-A-C

http://identifiers.org/hco/1/GRCh38#212967115-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190697836-A-C

212967117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 190697834-C-T

212967365-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 190697714-A-G

http://identifiers.org/hco/1/GRCh38#212967393-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190697696-A-C

212967393-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 190697696-A-T

212967410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 190697676-G-A

212967410-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 190697676-G-T

212967460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 190697622-A-G

212967474-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 190697608-G-T

212967500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 190697582-G-A

http://identifiers.org/hco/1/GRCh38#212967562-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190697549-A-C

212967562-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 190697549-A-G

212967562-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 190697549-A-T

212967589-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 190697520-T-G

212967637-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 190697473-A-G

http://identifiers.org/hco/1/GRCh38#212967671-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190697439-C-A

212967671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 190697439-C-T

212967865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 190697291-G-A

212967865-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 190697291-G-T

212967885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 190697270-G-A

212967885-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 190697270-G-T

212967897-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 190697258-G-T

212967951-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 190697203-A-G

212968060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 190697129-G-A

212968060-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 190697129-G-T

212968101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 190697091-A-G

212968112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 190697080-G-A

212968112-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 190697080-G-T

212968129-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 190697061-G-T

http://identifiers.org/hco/1/GRCh38#212968263-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#190696933-C-A

212968463-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 190695606-G-T

http://identifiers.org/hco/1/GRCh38#212968475-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#190695596-C-A

212968475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 190695596-C-T

212968520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 190695551-A-G

212968529-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 190695542-G-C

212968654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 190695435-C-T

212968658-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 190695431-G-A

212968658-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 190695431-G-T

212968667-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 190695422-T-C

212968690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 190695405-G-A

212968690-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 190695405-G-T

http://identifiers.org/hco/1/GRCh38#212968755-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#190695354-C-A

212968777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 190695344-T-C

212968815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 190695318-G-A

212968815-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 190695318-G-T

212968843-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 190695290-T-C

http://identifiers.org/hco/1/GRCh38#212968847-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190695286-C-A

212968847-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 190695286-C-G

212968847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 190695286-C-T

212968973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 190694954-A-G

212968988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 190694940-G-A

212968988-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 190694940-G-T

212968992-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 190694936-T-C

http://identifiers.org/hco/1/GRCh38#212969032-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190694907-C-A

212969032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 190694907-C-T

212969040-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 190694899-A-G

212969149-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 190694789-T-G

212969708-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190694750-T-G

212972284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190693157-G-A

212972295-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190693146-A-T

212972299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190693142-C-T

212972370-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190693075-T-A

212972480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190692966-G-A

212972528-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190692746-G-T

212972549-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190692705-C-G

212972549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190692705-C-T

http://identifiers.org/hco/1/GRCh38#212972824-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190692430-A-C

212972851-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 190692403-C-G

212972851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 190692403-C-T

212972986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190692275-C-T

http://identifiers.org/hco/1/GRCh38#212973353-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190691381-A-C

212973353-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190691381-A-G

212973353-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190691381-A-T

212973558-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 190691214-A-G

212973575-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 190691197-A-G

212973575-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 190691197-A-T

212973633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 190691147-G-A

212973633-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 190691147-G-C

212973633-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 190691147-G-T

212973663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 190691131-G-A

212973685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 190691111-G-A

http://identifiers.org/hco/1/GRCh38#212973717-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190691080-A-C

212973717-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 190691080-A-T

http://identifiers.org/hco/1/GRCh38#212973720-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190691077-A-C

212973803-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 190691015-T-C

212973871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 190690989-G-A

212973871-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 190690989-G-C

212973871-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 190690989-G-T

http://identifiers.org/hco/1/GRCh38#212973918-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190690961-A-C

212973926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 190690953-G-A

212973926-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 190690953-G-T

212973984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 190690895-G-A

212973984-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 190690895-G-T

212974012-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 190690867-C-G

http://identifiers.org/hco/1/GRCh38#212974042-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190690837-C-A

212974042-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 190690837-C-G

212974042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 190690837-C-T

http://identifiers.org/hco/1/GRCh38#212974136-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190690763-C-A

212974136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190690763-C-T

212974527-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190690549-T-C

http://identifiers.org/hco/1/GRCh38#212974551-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190690527-A-C

212974551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190690527-A-G

http://identifiers.org/hco/1/GRCh38#212974553-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190690525-C-A

212974553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 190690525-C-T

http://identifiers.org/hco/1/GRCh38#212974598-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190690497-C-A

212974628-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 190690462-T-C

http://identifiers.org/hco/1/GRCh38#212974782-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190690301-C-A

212974782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 190690301-C-T

212974863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 190690224-G-A

212974863-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 190690224-G-C

212974882-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 190690206-C-G

212974885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 190690203-G-A

212974975-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron variant
orthologous variants: 190690127-T-C

212974975-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron variant
orthologous variants: 190690127-T-G

212975046-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron variant
orthologous variants: 190690052-T-C

212975348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron variant
orthologous variants: 190689763-C-T

212975364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron variant
orthologous variants: 190689747-G-A

212975521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron variant
orthologous variants: 190688982-G-A

212975911-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron variant
orthologous variants: 190688662-A-G

212976342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron variant
orthologous variants: 190688309-A-G

212976784-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron variant
orthologous variants: 190687859-T-G

212976906-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron variant
orthologous variants: 190687740-G-T

212977064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron variant
orthologous variants: 190687596-G-A

212977064-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron variant
orthologous variants: 190687596-G-C

212977114-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron variant
orthologous variants: 190687552-T-C

212977202-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron variant
orthologous variants: 190687483-G-T

212977505-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron variant
orthologous variants: 190687200-T-C

212977512-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron variant
orthologous variants: 190687194-G-C

212977603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron variant
orthologous variants: 190687130-G-A

212978439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron variant
orthologous variants: 190686395-G-A

212978460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron variant
orthologous variants: 190686374-C-T

212978835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron variant
orthologous variants: 190686052-G-A

212978835-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron variant
orthologous variants: 190686052-G-T

212978979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron variant
orthologous variants: 190685917-G-A

212979286-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron_variant, undefined
orthologous variants: 190685619-A-G

http://identifiers.org/hco/1/GRCh38#212986642-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190684219-A-C

212986705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron variant
orthologous variants: 190684156-C-T

http://identifiers.org/hco/1/GRCh38#212986773-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190684106-A-C

http://identifiers.org/hco/1/GRCh38#212986782-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190684097-C-A

212986886-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron variant
orthologous variants: 190684046-A-G

212986948-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron variant
orthologous variants: 190683998-G-T

212987130-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron variant
orthologous variants: 190683732-G-T

212987137-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron variant
orthologous variants: 190683725-A-G

212987189-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron variant
orthologous variants: 190683684-T-G

212987876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron variant
orthologous variants: 190683321-G-A

212987917-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron variant
orthologous variants: 190683272-T-C

212988177-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron variant
orthologous variants: 190682991-G-T

http://identifiers.org/hco/1/GRCh38#212988297-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190682719-C-A

http://identifiers.org/hco/1/GRCh38#212988369-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190682665-C-A

http://identifiers.org/hco/1/GRCh38#212988425-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190682575-A-C

212988425-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron variant
orthologous variants: 190682575-A-G

212988470-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron variant
orthologous variants: 190682502-C-G

212988470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron variant
orthologous variants: 190682502-C-T

212988485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: intron variant
orthologous variants: 190682477-C-T

212988585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: 3 prime UTR variant
orthologous variants: 190682378-C-T

212988595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: 3 prime UTR variant
orthologous variants: 190682368-C-T

212988598-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: 3 prime UTR variant
orthologous variants: 190682365-G-C

212988713-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: 3 prime UTR variant
orthologous variants: 190682269-A-G

212988755-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: 3 prime UTR variant
orthologous variants: 190682241-A-G

http://identifiers.org/hco/1/GRCh38#212988764-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190682232-C-A

212988825-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: 3 prime UTR variant
orthologous variants: 190682170-T-C

http://identifiers.org/hco/1/GRCh38#212988826-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190682169-C-A

212988829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: 3 prime UTR variant
orthologous variants: 190682166-A-G

212988829-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: 3 prime UTR variant
orthologous variants: 190682166-A-T

212988832-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: 3 prime UTR variant
orthologous variants: 190682163-G-C

212988832-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: 3 prime UTR variant
orthologous variants: 190682163-G-T

212988898-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: 3 prime UTR variant
orthologous variants: 190682097-T-C

212989127-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 190681890-T-C

212989414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 190681617-A-G

212989654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 190681506-G-A

212989719-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 190681446-A-G

212989769-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 190681398-A-G

http://identifiers.org/hco/1/GRCh38#212989810-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190681344-C-A

http://identifiers.org/hco/1/GRCh38#212989853-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190681301-C-A

212989902-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 190681289-G-T

212989921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 190681271-T-C

212989951-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 190681241-A-G

http://identifiers.org/hco/1/GRCh38#212989965-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190681230-C-A

212989965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 190681230-C-T

http://identifiers.org/hco/1/GRCh38#212990016-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190681191-A-C

212990060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 190681161-G-A

212990060-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 190681161-G-C

212990060-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 190681161-G-T

http://identifiers.org/hco/1/GRCh38#212990267-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190681013-A-C

212990267-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 190681013-A-T

212990284-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 190680996-A-G

212990362-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 190680910-A-G

http://identifiers.org/hco/1/GRCh38#212990481-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190680841-C-A

212990591-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 190680779-A-G

http://identifiers.org/hco/1/GRCh38#212990663-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190680729-C-A

212990663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 190680729-C-T

212990870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 190680568-A-G

http://identifiers.org/hco/1/GRCh38#212990946-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190680500-C-A

http://identifiers.org/hco/1/GRCh38#212991597-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25723
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#190679926-C-A