98214624-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: 3 prime UTR variant
orthologous variants: 144130292-A-G

http://identifiers.org/hco/7/GRCh38#98214677-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144130327-C-A

98214677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: 3 prime UTR variant
orthologous variants: 144130327-C-T

http://identifiers.org/hco/7/GRCh38#98214692-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144130342-C-A

98214793-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: 3 prime UTR variant
orthologous variants: 144130386-G-T

98214807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: 3 prime UTR variant
orthologous variants: 144130399-G-A

98214807-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: 3 prime UTR variant
orthologous variants: 144130399-G-T

98214835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: 3 prime UTR variant
orthologous variants: 144130425-C-T

http://identifiers.org/hco/7/GRCh38#98214843-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144130433-C-A

98214952-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: 3 prime UTR variant
orthologous variants: 144130543-A-G

98215007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: 3 prime UTR variant
orthologous variants: 144130576-C-T

http://identifiers.org/hco/7/GRCh38#98215024-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144130617-C-A

98215024-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: 3 prime UTR variant
orthologous variants: 144130617-C-G

98215045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: 3 prime UTR variant
orthologous variants: 144130638-C-T

http://identifiers.org/hco/7/GRCh38#98215136-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144130795-C-A

98215136-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: 3 prime UTR variant
orthologous variants: 144130795-C-G

98215160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: 3 prime UTR variant
orthologous variants: 144130879-G-A

98215247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: 3 prime UTR variant
orthologous variants: 144131000-G-A

98215247-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: 3 prime UTR variant
orthologous variants: 144131000-G-T

98215294-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: 3 prime UTR variant
orthologous variants: 144131043-G-T

98215591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 144131354-G-A

98215591-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 144131354-G-T

http://identifiers.org/hco/7/GRCh38#98215729-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144131464-A-C

98215774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 144131495-G-A

98215793-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 144131503-T-A

98215900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 144131586-G-A

98216040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 144131685-G-A

98216040-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 144131685-G-T

98216050-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 144131693-G-T

98216052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 144131695-G-A

98216052-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 144131695-G-T

98216256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 144131802-G-A

98216256-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 144131802-G-T

http://identifiers.org/hco/7/GRCh38#98216364-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144131873-C-A

http://identifiers.org/hco/7/GRCh38#98216421-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144131926-A-C

98216421-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 144131926-A-G

98216429-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 144131934-A-G

http://identifiers.org/hco/7/GRCh38#98216476-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144131977-C-A

98216476-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 144131977-C-G

98216476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 144131977-C-T

98216480-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 144131981-T-C

98216748-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144132168-A-G

98216748-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144132168-A-T

98216807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144132216-G-A

98216807-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144132216-G-T

98216814-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 144132223-T-A

98216814-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 144132223-T-C

98216814-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 144132223-T-G

98216820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 144132229-T-C

98216904-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 144132299-C-G

98216904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 144132299-C-T

98216967-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 144132357-G-T

98217022-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 144132394-T-C

98217051-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 144132423-T-C

http://identifiers.org/hco/7/GRCh38#98217054-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144132426-C-A

98217054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 144132426-C-T

98217098-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 144132463-G-A

98217098-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 144132463-G-C

98217098-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 144132463-G-T

http://identifiers.org/hco/7/GRCh38#98217163-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144132523-C-A

98217163-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 144132523-C-G

98217163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 144132523-C-T

98217190-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 144132551-T-C

http://identifiers.org/hco/7/GRCh38#98217204-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144132567-C-A

98217204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 144132567-C-T

98217216-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 144132579-T-C

98217216-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 144132579-T-G

98217385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 144132729-G-A

98217385-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 144132729-G-T

98217665-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144132924-C-G

98217665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144132924-C-T

98217758-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 144133016-T-A

98217758-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 144133016-T-C

98217779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 144133037-G-A

98217779-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 144133037-G-T

98217891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144133124-G-A

98217901-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144133140-A-G

98217901-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144133140-A-T

http://identifiers.org/hco/7/GRCh38#98217913-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#144133152-C-A

98217913-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144133152-C-G

98217913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144133152-C-T

http://identifiers.org/hco/7/GRCh38#98217961-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#144133195-C-A

98217961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 144133195-C-T

98218063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144133297-G-A

98218063-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144133297-G-T

98218064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144133298-G-A

98218064-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144133298-G-C

98218064-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144133298-G-T

http://identifiers.org/hco/7/GRCh38#98218125-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144133347-C-A

98218125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144133347-C-T

http://identifiers.org/hco/7/GRCh38#98218128-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144133351-C-A

98218128-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144133351-C-G

98218128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144133351-C-T

98218263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144133449-C-T

98218319-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144133488-T-C

98221782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144134828-C-T

http://identifiers.org/hco/7/GRCh38#98221786-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144134841-C-A

98221787-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144134842-T-A

98221787-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144134842-T-C

98221787-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144134842-T-G

98221853-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144134933-G-T

98221858-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144134938-G-A

98221858-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144134938-G-C

98221858-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144134938-G-T

98221879-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144134967-G-C

98221985-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144135079-G-C

98222408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 144135395-G-A

98222408-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 144135395-G-T

http://identifiers.org/hco/7/GRCh38#98222425-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144135412-C-A

98222425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 144135412-C-T

98222432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 144135419-G-A

98222432-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 144135419-G-C

98222483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 144135470-G-A

98222483-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 144135470-G-C

98222543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144135535-G-A

98222543-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144135535-G-T

98222610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144135597-G-A

98222610-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144135597-G-T

98222625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144135612-G-A

98222625-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144135612-G-T

98222629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144135616-G-A

98222629-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144135616-G-T

http://identifiers.org/hco/7/GRCh38#98222638-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144135626-C-A

98222638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144135626-C-T

http://identifiers.org/hco/7/GRCh38#98222663-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144135653-C-A

98222663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144135653-C-T

98222670-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144135660-T-C

98222835-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144135800-T-G

98222840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144135805-G-A

98222840-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144135805-G-T

98222888-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144135843-T-G

http://identifiers.org/hco/7/GRCh38#98222898-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144135853-C-A

98222898-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144135853-C-G

98222898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144135853-C-T

98222926-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144135877-G-T

98222939-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144135902-C-G

98222967-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144135929-A-T

98222981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144135938-G-A

98222981-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144135938-G-C

98222981-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144135938-G-T

98222993-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 144135950-A-G

98223008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 144135965-C-T

98223143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 144136100-G-A

http://identifiers.org/hco/7/GRCh38#98223245-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144136200-C-A

98223252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144136207-G-A

98223252-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144136207-G-T

http://identifiers.org/hco/7/GRCh38#98223270-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144136225-C-A

98223270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144136225-C-T

98223459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144136360-G-A

98223464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144136363-G-A

http://identifiers.org/hco/7/GRCh38#98223871-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144136727-C-A

98223871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144136727-C-T

98224081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144136859-C-T

98224207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144136975-T-C

98224211-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144136979-G-C

http://identifiers.org/hco/7/GRCh38#98224289-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144137042-C-A

98224473-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144137234-T-C

98224538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144137294-G-A

98224656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144137472-G-A

98224656-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144137472-G-T

98224690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144137508-G-A

http://identifiers.org/hco/7/GRCh38#98224711-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144137526-C-A

98224715-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144137530-G-C

98224715-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144137530-G-T

98224758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144137571-A-G

98224787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144137617-A-G

98224787-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144137617-A-T

98224818-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 144137650-A-G

98224818-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 144137650-A-T

98224836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 144137668-G-A

98224836-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 144137668-G-T

http://identifiers.org/hco/7/GRCh38#98224839-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144137671-C-A

98224839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 144137671-C-T

98224897-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144137729-A-G

http://identifiers.org/hco/7/GRCh38#98224901-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144137733-A-C

98224901-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144137733-A-G

http://identifiers.org/hco/7/GRCh38#98225057-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144137881-C-A

98225057-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 144137881-C-G

98225057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 144137881-C-T

http://identifiers.org/hco/7/GRCh38#98225102-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144137926-C-A

98225121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144137947-G-A

98225121-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144137947-G-T

http://identifiers.org/hco/7/GRCh38#98227879-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144140104-C-A

98227958-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144140170-G-C

98227958-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144140170-G-T

98228028-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 144140240-T-A

98228028-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 144140240-T-C

98228157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144140375-C-T

98228158-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144140376-T-A

http://identifiers.org/hco/7/GRCh38#98228372-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144140629-C-A

98228372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144140629-C-T

http://identifiers.org/hco/7/GRCh38#98228379-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144140663-C-A

98228379-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144140663-C-G

http://identifiers.org/hco/7/GRCh38#98228388-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144140672-C-A

98228388-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144140672-C-G

98228388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144140672-C-T

http://identifiers.org/hco/7/GRCh38#98228394-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144140694-C-A

98228394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144140694-C-T

98228467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144140768-G-A

98228468-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144140769-G-T

98228500-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 144140801-T-C

98228500-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 144140801-T-G

98228506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 144140807-A-G

98228515-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144140816-A-G

98228518-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144140819-A-G

98228539-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144140841-T-C

98228595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144140896-G-A

98228595-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144140896-G-T

98228627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144140936-G-A

98228627-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144140936-G-T

http://identifiers.org/hco/7/GRCh38#98228690-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144140999-C-A

98228690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144140999-C-T

98228720-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 144141023-A-G

98228832-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144141169-G-T

http://identifiers.org/hco/7/GRCh38#98228852-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144141189-C-A

98228852-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144141189-C-G

http://identifiers.org/hco/7/GRCh38#98228915-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144141310-C-A

98228915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144141310-C-T

98228940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144141331-C-T

98228995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144141380-A-G

98229000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144141385-G-A

98229000-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144141385-G-C

98229000-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144141385-G-T

98229054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 144141458-C-T

98229159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 144141563-G-A

98229159-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 144141563-G-T

98229177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144141581-G-A

98229177-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144141581-G-T

98229189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144141583-G-A

98229221-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144141615-T-C

98229257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144141645-T-C

http://identifiers.org/hco/7/GRCh38#98229274-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144141659-C-A

98229288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144141673-G-A

98229288-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144141673-G-T

98229634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144141983-G-A

98229730-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144142051-T-C

98229730-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144142051-T-G

98230025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144142290-G-A

http://identifiers.org/hco/7/GRCh38#98230370-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144142440-C-A

98230509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144142581-C-T

98230540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144142599-C-T

98230717-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144142742-T-C

98230717-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144142742-T-G

http://identifiers.org/hco/7/GRCh38#98230832-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144142831-C-A

98230832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144142831-C-T

98230915-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144142935-G-T

http://identifiers.org/hco/7/GRCh38#98230924-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144142944-C-A

98230924-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144142944-C-G

98230924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144142944-C-T

98230928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144142948-C-T

http://identifiers.org/hco/7/GRCh38#98230941-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144142960-C-A

98230941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144142960-C-T

98231214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144143225-G-A

98231214-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144143225-G-T

98231266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 144143277-C-T

98231296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 144143307-G-A

98231371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 144143382-G-A

98231371-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, stop_gained
orthologous variants: 144143382-G-T

98231400-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144143411-G-T

98231861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 144144269-G-A

98231861-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 144144269-G-C

98231972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144144377-G-A

98231972-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144144377-G-T

http://identifiers.org/hco/7/GRCh38#98232065-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144144466-C-A

98232065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144144466-C-T

http://identifiers.org/hco/7/GRCh38#98232074-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144144482-C-A

98232074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144144482-C-T

98232081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144144489-G-A

98232081-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144144489-G-T

98232093-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144144505-A-G

http://identifiers.org/hco/7/GRCh38#98232565-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144145045-C-A

http://identifiers.org/hco/7/GRCh38#98232672-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144145144-A-C

98232701-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144145173-T-C

http://identifiers.org/hco/7/GRCh38#98232711-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144145190-A-C

98232713-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144145192-A-G

http://identifiers.org/hco/7/GRCh38#98232758-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144145226-C-A

http://identifiers.org/hco/7/GRCh38#98232765-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144145234-C-A

98232765-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144145234-C-G

98232765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144145234-C-T

98232777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144145270-G-A

98232777-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144145270-G-T

98232788-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144145374-A-G

98232819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 144145405-G-A

98232819-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 144145405-G-C

98232819-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 144145405-G-T

98232869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 144145455-C-T

98232920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 144145506-G-A

98232920-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 144145506-G-C

98232920-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 144145506-G-T

98232968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 144145554-C-T

98232971-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 144145557-G-C

98232971-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 144145557-G-T

98232979-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 144145565-G-T

98232995-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144145580-G-T

98233274-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144146558-G-T

98233277-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144146561-T-C

98233288-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144146572-T-C

http://identifiers.org/hco/7/GRCh38#98233305-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144146589-C-A

98233305-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144146589-C-G

98233305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144146589-C-T

http://identifiers.org/hco/7/GRCh38#98233366-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144146630-C-A

98233366-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144146630-C-G

98233366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144146630-C-T

http://identifiers.org/hco/7/GRCh38#98233367-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144146631-A-C

98233367-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144146631-A-G

98233413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 144146670-G-A

98233413-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 144146670-G-T

98233572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 144146829-G-A

98233572-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 144146829-G-C

98233651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 144146908-G-A

98233946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144147217-T-C

98234014-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144147258-T-C

98234025-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144147269-A-G

98234025-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144147269-A-T

98234037-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144147281-A-T

98234038-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144147282-A-G

http://identifiers.org/hco/7/GRCh38#98234165-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144147389-C-A

98234200-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144147444-T-G

98234329-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144147683-A-G

98234346-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144147700-G-T

http://identifiers.org/hco/7/GRCh38#98234384-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144147762-C-A

98234384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144147762-C-T

98236711-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144148160-T-C

98236832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 144148279-G-A

98236853-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 144148300-A-G

http://identifiers.org/hco/7/GRCh38#98236914-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144148361-C-A

98236914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144148361-C-T

98236928-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 144148375-G-C

98236928-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 144148375-G-T

http://identifiers.org/hco/7/GRCh38#98237004-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144148449-C-A

98237004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144148449-C-T

http://identifiers.org/hco/7/GRCh38#98238506-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144149384-C-A

98238506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144149384-C-T

98238527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 144149409-G-A

98238527-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144149409-G-T

98238587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 144149469-G-A

98238587-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144149469-G-C

98238587-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144149469-G-T

http://identifiers.org/hco/7/GRCh38#98238635-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144149516-C-A

98238635-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144149516-C-G

98238635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144149516-C-T

http://identifiers.org/hco/7/GRCh38#98238636-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144149517-C-A

98238636-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144149517-C-T

98238647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144149528-G-A

http://identifiers.org/hco/7/GRCh38#98240220-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144150460-C-A

98240220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144150460-C-T

98240838-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144150859-A-T

98240863-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 144150886-G-T

http://identifiers.org/hco/7/GRCh38#98240960-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144150983-C-A

98240960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144150983-C-T

98240979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144151001-G-A

http://identifiers.org/hco/7/GRCh38#98240991-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144151013-C-A

98241010-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144151031-A-G

http://identifiers.org/hco/7/GRCh38#98241062-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144151055-C-A

98241305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144151299-G-A

98241305-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144151299-G-T

98241307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144151301-G-A

http://identifiers.org/hco/7/GRCh38#98241338-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144151316-C-A

98241338-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144151316-C-G

http://identifiers.org/hco/7/GRCh38#98241373-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144151354-C-A

98241373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144151354-C-T

98241409-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144151385-T-A

98241640-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144151597-T-C

98241664-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144151630-G-C

http://identifiers.org/hco/7/GRCh38#98241682-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144151645-C-A

98241751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144151866-G-A

98241755-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144151873-C-G

98242155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144152203-G-A

98242232-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144152273-T-C

98242330-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144152379-G-C

98243009-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144152437-T-C

98243025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144152452-C-T

98243081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144152507-C-T

http://identifiers.org/hco/7/GRCh38#98243098-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144152523-C-A

98243229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144152619-G-A

98243335-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144152918-A-G

http://identifiers.org/hco/7/GRCh38#98243345-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144152926-A-C

98243345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144152926-A-G

98243346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144152927-G-A

98243346-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144152927-G-T

98243373-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144152954-T-A

98243373-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144152954-T-C

98243373-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144152954-T-G

98243390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144152972-C-T

98243399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144152981-T-C

98243399-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144152981-T-G

http://identifiers.org/hco/7/GRCh38#98243441-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144153028-A-C

98243441-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144153028-A-G

http://identifiers.org/hco/7/GRCh38#98243650-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144153257-C-A

98243650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144153257-C-T

http://identifiers.org/hco/7/GRCh38#98243661-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144153267-C-A

98243661-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144153267-C-G

98243661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144153267-C-T

98243704-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144153309-A-G

http://identifiers.org/hco/7/GRCh38#98243717-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144153322-C-A

98243730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144153332-G-A

98243730-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144153332-G-T

98243741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144153342-G-A

98243741-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144153342-G-T

98244446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144153559-G-A

98244446-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144153559-G-C

98244446-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144153559-G-T

http://identifiers.org/hco/7/GRCh38#98244455-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144153568-C-A

98244455-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144153568-C-G

98244455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144153568-C-T

98244464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144153577-G-A

98244464-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144153577-G-T

98244509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144153655-G-A

98244509-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144153655-G-T

98244541-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144153691-T-C

http://identifiers.org/hco/7/GRCh38#98244549-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144153699-A-C

http://identifiers.org/hco/7/GRCh38#98244550-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144153700-C-A

http://identifiers.org/hco/7/GRCh38#98244702-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144153852-C-A

98244702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144153852-C-T

http://identifiers.org/hco/7/GRCh38#98244703-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144153855-C-A

98244709-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144153861-A-T

98244767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144153933-G-A

98244767-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144153933-G-T

http://identifiers.org/hco/7/GRCh38#98244786-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144153969-C-A

98244786-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144153969-C-G

98244786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144153969-C-T

http://identifiers.org/hco/7/GRCh38#98244801-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144153985-C-A

98244803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144153987-G-A

98244815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144153995-C-T

http://identifiers.org/hco/7/GRCh38#98244851-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144154011-C-A

98244851-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144154011-C-G

98244954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 144154113-C-T

98245070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, stop_gained
orthologous variants: 144154229-G-A

98245119-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144154278-A-G

98245126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144154285-G-A

98245144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144154303-G-A

98245159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144154305-G-A

98245159-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144154305-G-T

http://identifiers.org/hco/7/GRCh38#98245165-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144154311-C-A

98245165-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144154311-C-G

98245165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144154311-C-T

http://identifiers.org/hco/7/GRCh38#98245166-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144154312-C-A

98245166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144154312-C-T

http://identifiers.org/hco/7/GRCh38#98245173-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144154318-C-A

98245173-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144154318-C-G

98245173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144154318-C-T

98245179-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144154324-G-T

98245210-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144154354-T-A

98245210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144154354-T-C

98245210-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144154354-T-G

http://identifiers.org/hco/7/GRCh38#98245245-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144154384-C-A

98245290-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144154420-A-G

98245427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144154555-C-T

98245527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144154735-C-T

98245557-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144154762-G-T

98245627-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144154862-A-G

98245675-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144154901-T-C

98245765-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144155004-C-G

98245765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144155004-C-T

98245766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144155005-G-A

98245781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144155020-A-G

98245781-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144155020-A-T

98245796-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144155036-G-T

98245797-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144155037-G-T

98245823-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144155078-G-T

98245828-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144155083-T-A

98245828-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144155083-T-C

98245832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144155087-G-A

98245832-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144155087-G-T

http://identifiers.org/hco/7/GRCh38#98245894-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#144155280-C-A

98245894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144155280-C-T

98245901-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144155287-T-A

98245976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 144155386-A-G

98245976-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained, undefined
orthologous variants: 144155386-A-T

98246038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 144155448-G-A

98246083-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144155493-C-G

98246151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144155561-G-A

http://identifiers.org/hco/7/GRCh38#98246172-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#144155584-C-A

98246172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 144155584-C-T

http://identifiers.org/hco/7/GRCh38#98246187-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#144155599-C-A

98246212-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144155623-G-C

98246212-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144155623-G-T

http://identifiers.org/hco/7/GRCh38#98246223-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#144155637-C-A

98246223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144155637-C-T

98248388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144156105-C-T

98248412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144156128-G-A

98249413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144156509-G-A

98249505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144156628-G-A

98250797-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144158174-C-G

98250797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144158174-C-T

98250823-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144158200-A-G

98250845-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144158218-T-C

98250861-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144158234-G-T

98250867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144158240-G-A

98250867-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 144158240-G-T

98250873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144158242-C-T

98250897-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144158266-G-T

98250924-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144158290-T-C

98251194-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144158540-A-G

98251248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144158589-G-A

98251248-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144158589-G-T

http://identifiers.org/hco/7/GRCh38#98251256-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144158597-C-A

http://identifiers.org/hco/7/GRCh38#98251269-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144158610-C-A

http://identifiers.org/hco/7/GRCh38#98251273-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144158614-C-A

98251273-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144158614-C-G

98251273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144158614-C-T

98251318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144159489-A-G

http://identifiers.org/hco/7/GRCh38#98251399-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144159566-C-A

98251400-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144159567-T-C

98251507-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 144159659-G-C

98251507-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 144159659-G-T

http://identifiers.org/hco/7/GRCh38#98251536-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144159688-C-A

98251536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 144159688-C-T

98251537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 144159689-G-A

98251537-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 144159689-G-T

98251540-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 144159692-A-G

98251572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144159724-G-A

98251575-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144159727-C-T

98251586-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144159738-G-T

98251637-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144159795-T-C

98251712-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144159859-T-A

http://identifiers.org/hco/7/GRCh38#98251790-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144159935-C-A

98251790-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 144159935-C-G

98251817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 144159968-G-A

98251817-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 144159968-G-T

98251821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 144159972-C-T

http://identifiers.org/hco/7/GRCh38#98251857-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144160009-C-A

98251858-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 144160010-T-C

http://identifiers.org/hco/7/GRCh38#98251924-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144160087-C-A

98252118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 144160305-G-A

98252118-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 144160305-G-T

http://identifiers.org/hco/7/GRCh38#98252142-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144160329-C-A

98252142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 144160329-C-T

98252156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 144160343-G-A

98252158-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 144160345-T-C

98252160-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 144160347-G-C

http://identifiers.org/hco/7/GRCh38#98252166-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22214
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#144160353-C-A