14810811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 91955960-G-A

14810811-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 91955960-G-C

14810811-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 91955960-G-T

14810815-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 91955964-T-C

14810836-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91955995-G-C

14810836-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91955995-G-T

14810879-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91956037-C-G

14810879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91956037-C-T

14811154-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91956153-G-C

14811200-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91956195-A-G

http://identifiers.org/hco/3/GRCh38#14811288-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#91956280-C-A

http://identifiers.org/hco/3/GRCh38#14811460-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91956389-C-A

http://identifiers.org/hco/3/GRCh38#14811464-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91956393-C-A

http://identifiers.org/hco/3/GRCh38#14811545-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91956441-C-A

14811545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91956441-C-T

14812619-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91957485-C-G

14812658-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91957527-T-A

14812759-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91957616-T-C

14812795-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91957656-A-G

14812909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91957760-G-A

14812924-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91957775-G-A

14812924-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91957775-G-C

14813002-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91957823-C-G

14813002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91957823-C-T

14813197-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91957991-G-T

14813355-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91958130-A-G

14813414-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91958190-C-G

14813604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91958382-A-G

14814116-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91958826-A-G

14814227-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91958896-A-G

14814323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91958985-C-T

14814448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91959121-C-T

14814927-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91959518-A-T

14814980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91959570-C-T

14814989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91959579-C-T

14815070-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91959648-T-A

14815254-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91959828-T-C

14815510-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91959915-A-G

14815708-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91960097-T-C

14815723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91960112-C-T

14815891-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91960263-T-C

14816091-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91960430-G-T

14816453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91960800-G-A

14816453-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91960800-G-T

14817471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91962205-C-T

14817697-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91962491-T-G

14817779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91962566-G-A

14817948-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91962674-T-C

14817984-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91962693-C-G

14817984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91962693-C-T

14818020-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91962723-T-G

14818115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91962812-C-T

14818325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91962972-C-T

14818332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91962978-C-T

14818396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91963042-C-T

14818403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91963072-C-T

14818422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91963090-T-C

14818948-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 91963774-T-A

http://identifiers.org/hco/3/GRCh38#14818949-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91963775-C-A

14818949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 91963775-C-T

14819034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 91963857-C-T

http://identifiers.org/hco/3/GRCh38#14819090-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91963913-C-A

14819090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 91963913-C-T

http://identifiers.org/hco/3/GRCh38#14819095-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91963918-C-A

14819095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 91963918-C-T

14819122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 91963945-C-T

14819275-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 91964083-C-G

14819275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 91964083-C-T

14819282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 91964090-G-A

14819282-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 91964090-G-T

http://identifiers.org/hco/3/GRCh38#14819347-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91964128-C-A

14819347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 91964128-C-T

14819380-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 91964146-A-G

14819402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 91964168-C-T

14819496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 91964253-C-T

14819504-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 91964261-G-C

14819669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 91964507-C-T

14819704-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 91964563-G-T

14819787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 91964619-C-T

http://identifiers.org/hco/3/GRCh38#14819818-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91964650-C-A

14819818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: synonymous variant
orthologous variants: 91964650-C-T

14819819-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: missense variant
orthologous variants: 91964651-A-T

14819952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: missense variant
orthologous variants: 91964778-G-A

14819980-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: synonymous variant
orthologous variants: 91964809-C-G

14819980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: synonymous variant
orthologous variants: 91964809-C-T

http://identifiers.org/hco/3/GRCh38#14820256-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91965100-C-A

14820256-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: synonymous variant
orthologous variants: 91965100-C-G

http://identifiers.org/hco/3/GRCh38#14820316-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91965163-C-A

14820316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: synonymous variant
orthologous variants: 91965163-C-T

14820335-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: synonymous variant
orthologous variants: 91965185-T-C

14820398-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: missense variant
orthologous variants: 91965239-G-C

14820613-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: synonymous variant
orthologous variants: 91965460-T-C

http://identifiers.org/hco/3/GRCh38#14820669-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91965516-C-A

14820838-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: missense variant
orthologous variants: 91965685-T-G

14820880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: synonymous variant
orthologous variants: 91965727-C-T

14820988-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: missense variant
orthologous variants: 91965835-G-C

http://identifiers.org/hco/3/GRCh38#14821117-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91965967-A-C

14821273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: synonymous variant
orthologous variants: 91966123-C-T

14821330-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: missense variant
orthologous variants: 91966180-C-G

14821531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: synonymous variant
orthologous variants: 91966381-C-T

http://identifiers.org/hco/3/GRCh38#14821609-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91966458-C-A

14821609-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, missense_variant
orthologous variants: 91966458-C-G

http://identifiers.org/hco/3/GRCh38#14821676-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91966511-C-A

14821676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91966511-C-T

14821739-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91966561-T-C

14821745-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91966567-T-C

14821745-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91966567-T-G

http://identifiers.org/hco/3/GRCh38#14821758-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91966580-C-A

14822252-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91966682-T-C

14822326-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91966782-A-G

14822661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91967075-C-T

14822691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91967093-C-T

14822709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91967120-G-A

14822800-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91967206-C-G

14822800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91967206-C-T

14822825-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91967236-G-T

14822908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91967303-G-A

14823128-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91967483-G-C

http://identifiers.org/hco/3/GRCh38#14823191-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91967545-A-C

14823201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91967553-C-T

14823311-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91967641-A-G

14823349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91967680-G-A

14823563-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91968057-T-C

14823641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91968131-A-G

14824082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91968534-G-A

14824348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91968728-G-A

14824411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91968776-G-A

14824486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91968793-G-A

14824555-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91968860-T-G

14824594-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91968900-G-C

14824801-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91969019-A-T

http://identifiers.org/hco/3/GRCh38#14824831-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91969049-A-C

14826628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91970161-G-A

14826790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91970325-C-T

14827624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91970945-C-T

http://identifiers.org/hco/3/GRCh38#14827625-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91970950-C-A

14827767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91971070-A-G

14828385-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91971493-T-A

14828483-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91971591-A-T

14828716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91971784-C-T

14829233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91971980-G-A

14829496-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91972208-T-G

14829504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91972216-C-T

14829647-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91972365-G-T

14829808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91972507-C-T

14829899-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91972548-C-G

14830024-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91972644-A-G

14830381-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91972971-A-G

14830415-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91973005-G-T

14830419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91973009-G-A

14831134-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91973693-G-T

14831304-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91975189-T-G

14831608-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91975437-A-G

http://identifiers.org/hco/3/GRCh38#14831913-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91975725-C-A

14831913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91975725-C-T

14832104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91975910-G-A

14832104-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91975910-G-T

14832265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91976038-C-T

14832322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91976086-G-A

14832326-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91976090-T-G

14832350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91976114-C-T

14832380-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91976137-G-T

14832479-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91976233-G-T

14832624-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91976343-C-G

14832625-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91976344-A-G

14832854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91976586-A-G

14832895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91976654-C-T

14832964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91976707-G-A

14832964-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91976707-G-C

14833134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91976914-G-A

14833259-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91977031-A-G

http://identifiers.org/hco/3/GRCh38#14833280-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91977052-C-A

14833281-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91977053-C-G

14833435-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91977219-A-G

14835561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91979406-G-A

14835646-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91979473-T-A

14835739-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91979577-T-G

14835749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91979587-G-A

14835987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91979764-G-A

14835987-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91979764-G-C

14836916-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91981137-T-C

14837082-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91981267-A-G

14837486-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91981656-A-G

14837621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91981793-C-T

14837809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91981995-G-A

14837809-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91981995-G-T

14837881-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91982034-G-T

14841400-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91986355-G-A

14841626-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91986559-T-A

14841890-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91986705-C-G

14841890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91986705-C-T

14841914-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91986725-C-G

14841914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91986725-C-T

14841928-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91986737-G-C

14842075-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91986880-G-A

14842096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91986904-G-A

14842194-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91986978-A-G

14842204-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91986988-C-G

http://identifiers.org/hco/3/GRCh38#14842394-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91987153-C-A

14842552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91987311-C-T

14843043-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91987799-T-C

14843394-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91988134-A-G

14843415-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91988155-T-C

14843451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91988181-G-A

14844311-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91989176-A-G

14844394-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91989257-G-T

14844577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91989420-C-T

14844659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91989481-C-T

14844768-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91989567-T-C

14844813-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91989611-A-G

14844872-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91989652-T-C

http://identifiers.org/hco/3/GRCh38#14844896-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91989680-A-C

14845005-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91989787-G-C

14845069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91989852-C-T

http://identifiers.org/hco/3/GRCh38#14845134-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91989913-C-A

14845134-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91989913-C-G

14845134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91989913-C-T

14845156-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91989933-C-G

14845236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91990027-G-A

14845293-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, undefined
orthologous variants: 91990067-C-G

14845293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, undefined
orthologous variants: 91990067-C-T

14845296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, undefined
orthologous variants: 91990070-C-T

http://identifiers.org/hco/3/GRCh38#14845317-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91990090-A-C

14845317-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91990090-A-G

14845570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91990313-C-T

14846049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91990475-T-C

14846101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91990518-G-A

14846167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91990578-C-T

14846273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91990656-G-A

14846879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91991212-G-A

14846992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91991304-C-T

14847296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91991583-G-A

14847312-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91991599-T-C

14847625-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91991843-A-G

14847722-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91991919-G-C

14847751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91991946-C-T

14848002-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91992036-A-G

14848039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91992074-C-T

14848040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91992075-G-A

14848040-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91992075-G-T

14848213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91992246-C-T

14848256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91992286-C-T

14849078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91994512-T-C

14849148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91994609-C-T

14849470-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91994924-A-G

14849914-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91995454-G-T

14849997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91995506-C-T

14850046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91995541-G-A

14850146-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91995637-T-G

14850158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91995649-C-T

14850320-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91995762-C-G

14850699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91996149-C-T

14851644-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91997195-A-G

14851692-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91997246-C-G

14851692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91997246-C-T

14851942-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91997449-A-G

14851946-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91997453-T-A

14851971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91997478-G-A

14852022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91997520-C-T

http://identifiers.org/hco/3/GRCh38#14852505-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91997951-A-C

14852543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91997980-G-A

http://identifiers.org/hco/3/GRCh38#14852619-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91998057-C-A

14852619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91998057-C-T

14852713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91998130-G-A

14852918-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91998316-G-C

14853060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91998438-G-A

14853440-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91998671-C-G

14853611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91998794-G-A

14857640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91999612-A-G

14857773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 91999730-C-T

http://identifiers.org/hco/3/GRCh38#14857946-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#91999891-C-A

14864011-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 92001400-T-C

14864011-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 92001400-T-G

http://identifiers.org/hco/3/GRCh38#14864128-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: missense_variant, splice_region_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#92001485-C-A

14864128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: splice_region_variant, synonymous_variant, undefined
orthologous variants: 92001485-C-T

14864339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 92001701-C-T

http://identifiers.org/hco/3/GRCh38#14864392-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92001741-C-A

14864393-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 92001742-T-C

14865252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 92002189-C-T

14865421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 92002355-G-A

14865513-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 92003072-T-C

14865535-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 92003098-C-G

14865535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 92003098-C-T

http://identifiers.org/hco/3/GRCh38#14865573-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92003144-C-A

14865703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 92003278-A-G

http://identifiers.org/hco/3/GRCh38#14865745-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92003316-C-A

14865852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 92003397-G-A

14865901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 92003445-C-T

14866245-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 92003634-T-C

14866709-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 92003948-T-C

14867292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 92004754-G-A

14867527-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 92005040-T-C

14867544-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 92005057-T-G

14867616-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 92005124-C-T

14867617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 92005125-C-T

14867625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 92005133-C-T

http://identifiers.org/hco/3/GRCh38#14867684-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92005183-C-A

14867684-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 92005183-C-G

14867684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 92005183-C-T

14867685-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 92005184-T-G

14867686-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 92005185-G-C

14867686-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 92005185-G-T

14867753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 92005247-C-T

14867815-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 92005302-A-G

14867818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 92005305-G-A

14867934-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 92005410-G-C

14868271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 92005732-C-T

14868344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 92005800-G-A

14868349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 92005805-C-T

14868377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 92005834-C-T

14868429-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 92005869-G-T

14868438-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 92005878-G-C

14870497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 92007382-C-T

14870498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 92007383-T-C

14870790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 92007578-C-T

14870803-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 92007591-A-G

14870811-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 92007599-C-G

http://identifiers.org/hco/3/GRCh38#14870825-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92007613-C-A

14870825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 92007613-C-T

14870894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 92007661-C-T

14871209-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 92007912-A-G

14871352-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 92008012-G-C

14871352-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 92008012-G-T

14871357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 92008017-G-A

14871357-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 92008017-G-C

14871368-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 92008028-T-C

14871680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 92008233-C-T

14872025-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 92008473-A-G

14872030-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 92008478-A-T

14873654-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 92009401-G-T

14873664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 92009411-G-A

14876955-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 92011711-G-T

14877063-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 92011813-A-G

14877155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, undefined
orthologous variants: 92011907-C-T

14877416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 92012141-G-A

14877576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 92012294-G-A

14877583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 92012301-C-T

14879104-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 92014591-T-G

14880450-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 92014903-A-G

14880450-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 92014903-A-T

14880680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 92015107-C-T

14880692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 92015119-C-T

http://identifiers.org/hco/3/GRCh38#14880697-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92015124-A-C

14881058-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 92015442-A-G

14881097-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 92015493-G-T

14881100-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 92015496-A-T

14881196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 92015620-A-G

14881414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 92015739-A-G

14881460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 92015787-C-T

14881472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 92015799-C-T

14881506-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 92015831-T-C

14881506-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 92015831-T-G

14881755-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 92015963-C-G

14882002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 92016171-G-A

14882144-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 92016292-G-C

14882161-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 92016309-A-T

14882224-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 92016362-T-C

14882250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 92016385-G-A

14882250-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron variant
orthologous variants: 92016385-G-T

14885561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92018317-G-A

14885574-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92018330-G-A

14885574-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92018330-G-T

14886409-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92019150-T-C

14897168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92026742-C-T

14897175-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92026749-G-T

http://identifiers.org/hco/3/GRCh38#14897198-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92026771-C-A

14897205-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92026778-G-T

14897335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92026855-G-A

14897335-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92026855-G-T

14897399-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92026918-A-T

http://identifiers.org/hco/3/GRCh38#14897400-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92026919-C-A

14897400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92026919-C-T

http://identifiers.org/hco/3/GRCh38#14897419-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92026932-C-A

14897419-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92026932-C-G

14897421-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92026934-G-T

14897422-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92026935-G-T

14897569-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 92027047-T-C

14897804-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92027282-G-T

14897812-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92027290-T-G

14897865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92027303-A-G

14897865-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92027303-A-T

14897874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92027311-G-A

14897874-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92027311-G-T

14897944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 92027379-G-A

14897944-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 92027379-G-T

14897959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 92027394-C-T

14897977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 92027412-G-A

14898029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 92027464-C-T

14898036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 92027471-C-T

14898068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 92027503-G-A

14898068-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 92027503-G-T

http://identifiers.org/hco/3/GRCh38#14898120-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92027554-C-A

14898227-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92027664-A-G

14898229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92027666-G-A

14898229-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92027666-G-T

14898305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92027734-G-A

http://identifiers.org/hco/3/GRCh38#14898513-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92027920-C-A

14898599-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92027976-A-G

http://identifiers.org/hco/3/GRCh38#14898671-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92028008-C-A

14898671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92028008-C-T

14898674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92028011-C-T

14898709-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92028034-A-T

14898720-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92028045-T-C

14898720-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92028045-T-G

14898892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92028186-G-A

14898892-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92028186-G-T

http://identifiers.org/hco/3/GRCh38#14898894-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92028188-A-C

14898898-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92028193-G-T

14898929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92028219-G-A

14898929-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92028219-G-T

14898956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92028248-G-A

14898956-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92028248-G-T

14899029-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92028283-G-T

http://identifiers.org/hco/3/GRCh38#14899036-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92028290-C-A

14899061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92028313-C-T

14899217-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92028443-G-C

14899245-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92028469-T-C

14900076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92029920-G-A

14900076-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92029920-G-T

14900095-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92029939-C-G

14900192-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92030043-T-G

14900341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92030147-G-A

14900362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92030165-C-T

14900380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92030185-C-T

14900473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92030278-G-A

14900473-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92030278-G-T

14900474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92030279-G-A

14900474-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92030279-G-T

14900546-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92030342-A-T

14900577-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92030374-T-G

http://identifiers.org/hco/3/GRCh38#14900578-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92030375-C-A

14900585-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92030382-T-A

14900586-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92030383-G-T

http://identifiers.org/hco/3/GRCh38#14900593-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92030390-C-A

14900593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92030390-C-T

14900649-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92030447-C-G

http://identifiers.org/hco/3/GRCh38#14900844-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92030618-A-C

http://identifiers.org/hco/3/GRCh38#14900908-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92030641-C-A

14900929-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92030661-G-C

14900999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 92030788-C-T

14901022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 92030811-C-T

14901106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92030893-G-A

14901111-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92030897-T-C

http://identifiers.org/hco/3/GRCh38#14901118-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92030904-C-A

14901118-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92030904-C-G

14901181-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92030946-G-A

14901181-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92030946-G-C

14901181-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92030946-G-T

14901199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92030964-G-A

14901199-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92030964-G-T

14902552-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92031495-A-T

14902566-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92031509-A-G

14902641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92031576-C-T

14907498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92038645-T-C

14907498-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92038645-T-G

14907504-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92038651-A-G

14907504-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92038651-A-T

http://identifiers.org/hco/3/GRCh38#14907514-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92038661-A-C

14907514-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92038661-A-G

14907524-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92038671-G-C

14907524-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92038671-G-T

14907552-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92038701-A-G

http://identifiers.org/hco/3/GRCh38#14907554-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92038703-C-A

14907554-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92038703-C-G

14907588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92038735-A-G

14907816-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92038952-G-A

14907816-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92038952-G-T

14907817-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92038953-T-G

14907875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92038999-C-T

14907896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92039014-G-A

14908087-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92039207-T-A

14908385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92039563-G-A

14908392-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92039570-C-T

14908412-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92039590-A-G

14910831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92039786-G-A

14910831-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92039786-G-T

http://identifiers.org/hco/3/GRCh38#14910992-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92039932-C-A

14911008-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92039948-G-C

14911099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92040038-G-A

14911140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92040082-G-A

14916624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92041586-T-C

14916692-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92041653-C-G

14916692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92041653-C-T

14916801-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92041738-T-A

14916829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92041761-G-A

14916907-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92041835-A-G

http://identifiers.org/hco/3/GRCh38#14917002-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92041927-A-C

14917216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92042095-C-T

14917260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 92042140-G-A

14917405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92042292-G-A

14917405-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92042292-G-T

14917429-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92042300-T-C

14917456-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92042326-T-A

14917456-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92042326-T-C

http://identifiers.org/hco/3/GRCh38#14918668-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92043068-C-A

14918668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92043068-C-T

14918673-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92043073-G-C

14918673-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92043073-G-T

14918740-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92043146-T-C

14918740-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92043146-T-G

14918741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92043147-G-A

14921943-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92044508-T-A

14921943-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92044508-T-C

14922020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92044585-G-A

14922020-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92044585-G-T

14922067-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92044605-T-A

14922126-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92044660-T-G

http://identifiers.org/hco/3/GRCh38#14922161-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92044702-C-A

14922161-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92044702-C-G

14922161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92044702-C-T

14922222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92044744-T-C

14922268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92044772-G-A

14922268-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92044772-G-T

http://identifiers.org/hco/3/GRCh38#14922288-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92044788-C-A

14922288-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92044788-C-G

14922356-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92044820-T-C

14922365-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92044824-T-C

14922368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92044827-C-T

http://identifiers.org/hco/3/GRCh38#14922369-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92044828-C-A

14922369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92044828-C-T

14922370-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92044829-T-A

14922572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92045025-G-A

14922572-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92045025-G-T

http://identifiers.org/hco/3/GRCh38#14922609-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92045057-C-A

14922609-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92045057-C-G

14922609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92045057-C-T

14922657-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92045081-A-G

14922661-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92045085-T-C

14922669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92045093-G-A

14922748-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92045170-C-G

14922777-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92045194-A-T

14922795-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92045212-A-G

14922862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92045272-C-T

14922863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92045273-G-A

http://identifiers.org/hco/3/GRCh38#14922911-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92045328-C-A

14922911-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92045328-C-G

14922911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92045328-C-T

14923039-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 92045423-C-G

14923187-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92045571-A-G

14923187-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92045571-A-T

http://identifiers.org/hco/3/GRCh38#14923252-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92045633-C-A

14923252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92045633-C-T

14923410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92045812-C-T

14923490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92045942-C-T

14923990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 92046331-G-A

14924114-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 92046458-G-T

http://identifiers.org/hco/3/GRCh38#14924120-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#92046464-C-A

14924120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 92046464-C-T

http://identifiers.org/hco/3/GRCh38#14924315-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92046637-C-A

14924315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92046637-C-T

14924357-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92046709-C-G

14924525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92046865-C-T

14924543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92046880-G-A

http://identifiers.org/hco/3/GRCh38#14924592-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92046929-C-A

14924592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92046929-C-T

14926137-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92048360-A-G

14926301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92048475-G-A

14926301-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92048475-G-T

14926303-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92048478-T-G

http://identifiers.org/hco/3/GRCh38#14926308-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92048483-C-A

14926591-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92048731-C-G

14932757-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92051256-T-C

14932757-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92051256-T-G

14932886-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92051356-A-G

14932933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92051400-T-C

14932953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92051420-C-T

14933211-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92051631-A-G

http://identifiers.org/hco/3/GRCh38#14933241-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92051661-C-A

14933344-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92051714-G-T

14933467-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 92051828-T-C

14933467-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 92051828-T-G

14933468-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 92051829-G-T

14933472-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 92051833-A-G

http://identifiers.org/hco/3/GRCh38#14933613-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92051986-A-C

14933613-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 92051986-A-G

http://identifiers.org/hco/3/GRCh38#14933671-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92052041-C-A

14933698-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 92052047-G-T

14934054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 92052228-G-A

http://identifiers.org/hco/3/GRCh38#14934096-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92052269-C-A

14934116-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 92052285-A-G

14934328-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 92052511-A-G

14934430-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 92052611-A-G

http://identifiers.org/hco/3/GRCh38#14934462-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19117
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92052642-C-A