14070966-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, undefined
orthologous variants: 13074039-T-G

14071102-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, undefined
orthologous variants: 13074170-G-T

14071200-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron variant
orthologous variants: 13074255-C-G

14071200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron variant
orthologous variants: 13074255-C-T

14071215-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, undefined
orthologous variants: 13074270-A-G

14071252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron variant
orthologous variants: 13074295-G-A

14071353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 13074406-G-A

14071353-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 13074406-G-C

14071353-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 13074406-G-T

14071363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, splice_region_variant, undefined
orthologous variants: 13074416-G-A

14071363-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, splice_region_variant, undefined
orthologous variants: 13074416-G-T

14071367-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_donor_variant, undefined
orthologous variants: 13074420-T-C

14071367-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_donor_variant, undefined
orthologous variants: 13074420-T-G

14071379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 13074432-G-A

14071379-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 13074432-G-T

14071391-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 13074449-T-C

14071391-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 13074449-T-G

14071396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 13074453-G-A

14071396-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 13074453-G-T

14071401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 13074458-G-A

14071401-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 13074458-G-T

http://identifiers.org/hco/16/GRCh38#14071417-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#13074473-C-A

14071417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13074473-C-T

http://identifiers.org/hco/16/GRCh38#14071456-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#13074512-C-A

14071456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 13074512-C-T

http://identifiers.org/hco/16/GRCh38#14072145-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#13075144-A-C

14072145-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13075144-A-G

14072266-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13075235-A-G

14073126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13075793-C-T

http://identifiers.org/hco/16/GRCh38#14073259-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#13075905-A-C

14074004-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13076555-C-G

14074105-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13076640-G-C

14074158-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13076693-G-T

14074358-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13076901-A-T

14075044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13077602-C-T

14075170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13077725-A-G

http://identifiers.org/hco/16/GRCh38#14075334-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#13077863-C-A

14075358-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 13077886-A-G

14075797-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13078453-A-G

14078883-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13082643-A-G

14079247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13082900-G-A

14079344-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 13082993-T-C

14079344-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 13082993-T-G

14079387-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13083041-A-G

http://identifiers.org/hco/16/GRCh38#14079419-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#13083054-C-A

14079419-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13083054-C-G

14079423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13083058-C-T

14079452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13083086-G-A

14079452-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13083086-G-C

14079461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13083095-A-G

14086981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13083693-C-T

14087042-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13083746-A-G

14087520-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13084138-T-C

14087530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13084148-G-A

14088134-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13084710-G-C

14088270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 13084836-C-T

14088337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 13084867-G-A

http://identifiers.org/hco/16/GRCh38#14088743-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#13085238-A-C

14088743-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13085238-A-G

14088777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13085270-G-A

14089042-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13085535-T-C

14089310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13085785-C-T

14090770-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13087339-A-G

14091343-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13087849-T-C

http://identifiers.org/hco/16/GRCh38#14091449-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#13087946-C-A

14091504-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13087997-A-G

http://identifiers.org/hco/16/GRCh38#14091637-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#13088098-C-A

14091651-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13088112-T-A

14092703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13092000-C-T

14095287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13093020-G-A

14095561-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13093274-G-T

14096028-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13093411-A-G

14097061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13094098-C-T

14097143-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13094167-A-G

14097452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 13094479-G-A

14097490-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 13094516-T-C

14097503-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 13094527-G-T

http://identifiers.org/hco/16/GRCh38#14100357-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#13108318-A-C

14100587-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13108569-A-G

14100812-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13108804-A-G

14101206-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13109302-C-G

14101206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13109302-C-T

14101691-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13110127-T-C

14101750-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13110170-T-A

14101919-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13110316-C-G

14101963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13110355-A-G

http://identifiers.org/hco/16/GRCh38#14102313-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#13110845-C-A

14103011-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13111466-A-G

14103048-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13111500-T-C

14103632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13112014-C-T

14103634-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13112016-C-G

14104163-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13112408-T-G

14105734-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13114230-T-A

14105790-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13114287-C-G

14105790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13114287-C-T

14106006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13114505-G-A

14106025-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13114521-A-G

14106025-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13114521-A-T

14106169-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13114633-A-G

14106796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13115129-G-A

http://identifiers.org/hco/16/GRCh38#14107034-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#13115358-A-C

14107132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13115405-C-T

14107970-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13115905-G-T

http://identifiers.org/hco/16/GRCh38#14108083-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#13115978-A-C

14108182-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13116014-T-A

14108347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13116167-C-T

14108763-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13116579-T-A

14108944-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13116753-C-G

14108944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13116753-C-T

14109057-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13116869-T-C

14109070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13116883-G-A

14109256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13117066-G-A

14109345-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13117151-T-C

14109431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13117239-G-A

14110411-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13117665-G-C

14110760-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 13117927-T-C

14110922-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13118086-A-T

http://identifiers.org/hco/16/GRCh38#14110952-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#13118116-C-A

14111298-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13119721-G-C

14111494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13119912-C-T

14111653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13120052-A-G

14111708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13120109-G-A

14111936-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13120379-C-G

14112152-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13120585-T-G

14112339-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13120773-G-T

14112369-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13120814-A-G

14114211-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13124081-T-C

http://identifiers.org/hco/16/GRCh38#14114252-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#13124128-A-C

14114368-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13124231-A-T

14114491-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13124338-T-C

14114731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13124551-G-A

14115144-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13124923-T-C

http://identifiers.org/hco/16/GRCh38#14115550-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#13125296-C-A

14115550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13125296-C-T

14120728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13126588-C-T

14121002-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13126803-A-G

14121120-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13126885-G-T

14121282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13127033-G-A

14121610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13127318-G-A

14122194-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13127790-A-T

http://identifiers.org/hco/16/GRCh38#14122252-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#13127832-A-C

14122252-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13127832-A-T

14125468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13128351-G-A

14125807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13128679-T-C

14125815-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13128688-A-G

14125867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13128740-C-T

14126641-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13130117-T-C

14126649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13130125-G-A

14133569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13137567-C-T

http://identifiers.org/hco/16/GRCh38#14133934-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#13138002-A-C

14133934-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13138002-A-G

http://identifiers.org/hco/16/GRCh38#14134031-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#13138084-A-C

14134105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13138142-G-A

14136863-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13141771-G-C

14137227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13142133-C-T

14137439-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13142340-A-T

14137482-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13142383-T-A

14137551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13142453-A-G

14137688-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13142592-C-G

14137750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13142634-G-A

14137765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13142649-A-G

14137933-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13142830-C-G

14138311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13143174-C-T

14138374-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13143216-C-G

14138594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13143387-C-T

14138779-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13143505-T-G

14140045-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13143788-A-G

14140129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13143849-C-T

14140142-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13143862-G-A

14140174-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13143896-T-C

14140262-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13143980-A-T

14140480-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13144174-T-C

http://identifiers.org/hco/16/GRCh38#14140512-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#13144206-A-C

14140512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13144206-A-G

14140533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13144223-T-C

14140895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 13144545-G-A

14140895-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 13144545-G-T

14140903-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 13144553-T-C

14140936-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 13144586-G-T

14141088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 13144726-G-A

14141088-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 13144726-G-T

14141115-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 13144748-T-C

14141143-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 13144776-A-G

14141169-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 13144806-A-G

http://identifiers.org/hco/16/GRCh38#14141299-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#13144924-C-A

14145189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13147038-G-A

14145654-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13147331-G-T

14145871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13147479-A-G

14145980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13147588-G-A

14146095-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13147663-G-C

14146175-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13147759-A-G

14146351-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13147919-T-C

14146624-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13148186-C-G

14147069-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13148510-A-G

14147157-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13148572-G-C

14147187-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13148593-C-G

14147671-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13149052-A-G

14147835-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13149207-A-G

14147966-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13149337-A-G

14148531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13149670-G-A

14148833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13150039-G-A

http://identifiers.org/hco/16/GRCh38#14151540-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#13151490-C-A

14151567-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 13151526-A-G

14151615-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 13151573-A-G

14151646-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 13151603-T-G

14151741-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 13151691-T-C

14152076-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 13152022-G-T

14152082-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 13152028-T-C

14152292-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 13152229-C-G

http://identifiers.org/hco/16/GRCh38#14152483-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#13152381-A-C

14152484-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 13152382-T-A

14152558-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 13152467-T-A

14152671-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 13152592-C-G

14152714-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 13152633-G-T

14152774-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 13152690-T-G

14152791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 13152708-G-A

14152791-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 13152708-G-T

14156505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13155645-C-T

14156836-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13155965-A-G

http://identifiers.org/hco/16/GRCh38#14157952-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#13157239-A-C

http://identifiers.org/hco/16/GRCh38#14158134-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#13157391-A-C

14158134-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13157391-A-G

14158353-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13157582-G-C

http://identifiers.org/hco/16/GRCh38#14158452-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#13157653-A-C

14158556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13157734-A-G

14158736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13157894-G-A

14158874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13158014-G-A

14158999-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13158138-G-C

http://identifiers.org/hco/16/GRCh38#14159146-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#13158314-A-C

14159305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13158471-T-C

14159581-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13158962-A-G

14165662-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13161770-C-G

http://identifiers.org/hco/16/GRCh38#14181218-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#13171589-A-C

14181582-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13171877-A-G

14181726-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 13171970-C-G

14181878-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13172118-A-G

14182310-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13172512-T-C

14182337-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13172540-T-C

14182532-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13172753-A-G

14183405-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13173487-T-G

14183473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13173542-G-A

http://identifiers.org/hco/16/GRCh38#14183816-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#13174031-A-C

14183922-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13174120-A-G

14183999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13174175-A-G

14184020-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13174188-A-T

http://identifiers.org/hco/16/GRCh38#14184537-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#13174342-C-A

14184933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13174689-C-T

14185099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13174829-G-A

14185408-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13175142-G-T

14186031-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13175646-T-C

14186237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13175844-A-G

14186748-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_donor_variant, undefined
orthologous variants: 13176351-T-G

14187442-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13177019-C-T

14187523-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13177081-T-A

14188489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13177996-A-G

14189391-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13178880-T-C

14189862-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13179349-T-C

14190297-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13180239-A-G

14190322-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13180267-T-C

14190327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13180272-C-T

14190361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13180310-C-T

14190419-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13180324-G-T

14190564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13180468-T-C

14190678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13180584-C-T

14190757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13180631-G-A

14190899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-A

14191320-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13181138-G-C

14191380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13181200-C-T

http://identifiers.org/hco/16/GRCh38#14191898-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: -C-A

14192048-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13181604-T-C

14192380-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13181643-G-C

14192840-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13182216-T-C

14192961-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13182308-T-A

14193090-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13182400-G-C

14193168-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13182459-G-C

14193356-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 13182550-A-G

14193557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 13182670-C-T

http://identifiers.org/hco/16/GRCh38#14193570-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#13182683-C-A

14193570-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 13182683-C-G

14193740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 13182836-G-A

14193740-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 13182836-G-T

14193759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 13182854-C-T

14193788-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 13182883-A-G

http://identifiers.org/hco/16/GRCh38#14193877-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#13182980-C-A

http://identifiers.org/hco/16/GRCh38#14194067-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#13183046-A-C

14194351-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 13183301-A-G

14194790-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 13183579-T-G

14195376-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 13184152-A-T

http://identifiers.org/hco/16/GRCh38#14195490-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#13184278-C-A

14195490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 13184278-C-T

14195748-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13184586-T-C

http://identifiers.org/hco/16/GRCh38#14195950-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#13184782-A-C

14196061-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13184982-T-C

14196078-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13184999-A-T

14196188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13185103-G-A

14196290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13185204-G-A

14196290-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13185204-G-C

http://identifiers.org/hco/16/GRCh38#14196570-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#13185357-A-C

14197933-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13186546-T-A

14198315-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13187467-C-G

14198315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13187467-C-T

14198625-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13187717-T-C

14198866-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13187911-T-A

14198866-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13187911-T-C

14199349-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13188114-T-G

14199449-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13188186-A-G

14199504-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13188230-T-G

14199774-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13188384-T-G

14199910-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13188476-T-C

http://identifiers.org/hco/16/GRCh38#14200075-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#13188621-C-A

14202299-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13188932-T-G

14202683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13189462-T-C

14203137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13189850-G-A

14205361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13191140-G-A

14205466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13191215-T-C

14205583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13191315-G-A

14205705-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13191416-C-G

14205795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13191518-G-A

14205795-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13191518-G-C

14205886-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13191599-G-T

14206025-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13191728-C-G

http://identifiers.org/hco/16/GRCh38#14206519-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#13192097-A-C

14207596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13193607-G-A

14208534-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13194487-A-G

14209166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13195045-C-T

14209262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13195141-C-T

14209263-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13195142-A-G

14209910-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13195692-A-G

14209931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13195716-C-T

14209985-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13195770-C-G

14210043-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13195820-A-G

14210140-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13195921-T-C

http://identifiers.org/hco/16/GRCh38#14210207-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#13196077-C-A

14210207-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13196077-C-G

14210207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13196077-C-T

http://identifiers.org/hco/16/GRCh38#14210366-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#13196247-A-C

14210366-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13196247-A-G

14210375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13196256-C-T

14210779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13196628-C-T

14211992-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13197392-A-T

14212465-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13197792-A-G

14212538-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13197859-A-G

14212548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13197869-G-A

14212556-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13197877-T-C

14212576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13197895-C-T

14212974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13198789-G-A

14212975-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13198790-A-G

14213449-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13199322-A-G

14213702-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13199527-T-C

14214381-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13200061-A-G

14214491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13200128-A-G

14214523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13200161-G-A

14214819-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13200395-G-C

14214819-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13200395-G-T

14214976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron variant
orthologous variants: 13200545-C-T

14215091-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron variant
orthologous variants: 13200671-A-G

14215466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron variant
orthologous variants: 13201183-G-A

14215596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron variant
orthologous variants: 13201279-C-T

14216404-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron variant
orthologous variants: 13201463-T-A

14216902-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron variant
orthologous variants: 13201928-C-G

14217083-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron variant
orthologous variants: 13202021-A-G

14217346-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron variant
orthologous variants: 13202275-A-G

14217348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron variant
orthologous variants: 13202277-A-G

http://identifiers.org/hco/16/GRCh38#14217372-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#13202301-A-C

14217376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron variant
orthologous variants: 13202305-A-G

14217383-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron variant
orthologous variants: 13202312-G-C

14217383-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron variant
orthologous variants: 13202312-G-T

14217396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron variant
orthologous variants: 13202324-G-A

14217396-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron variant
orthologous variants: 13202324-G-T

14218838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: missense variant
orthologous variants: 13203488-A-G

14218842-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: synonymous variant
orthologous variants: 13203492-C-G

14218846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: missense variant
orthologous variants: 13203496-A-G

14218846-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: missense variant
orthologous variants: 13203496-A-T

14218851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: synonymous variant
orthologous variants: 13203501-G-A

14218858-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: missense variant
orthologous variants: 13203508-T-C

14218858-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: missense variant
orthologous variants: 13203508-T-G

14218905-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: synonymous variant
orthologous variants: 13203555-T-C

14218908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: synonymous variant
orthologous variants: 13203558-G-A

14218935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: synonymous variant
orthologous variants: 13203585-G-A

14218984-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: missense variant
orthologous variants: 13203634-A-G

14219692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron variant
orthologous variants: 13204812-C-T

14219694-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron variant
orthologous variants: 13204814-T-C

14219891-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron variant
orthologous variants: 13205031-A-G

http://identifiers.org/hco/16/GRCh38#14221130-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#13206060-C-A

14232007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron variant
orthologous variants: 13210896-C-T

14232112-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron variant
orthologous variants: 13211015-T-C

14232416-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron variant
orthologous variants: 13211241-G-C

14232437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron variant
orthologous variants: 13211262-C-T

14234122-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron variant
orthologous variants: 13212663-G-C

14234122-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron variant
orthologous variants: 13212663-G-T

14234232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: synonymous variant
orthologous variants: 13212773-C-T

14234481-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron variant
orthologous variants: 13212993-G-C

14234926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron variant
orthologous variants: 13213403-G-A

14235145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron variant
orthologous variants: 13213637-G-A

14235151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron variant
orthologous variants: 13213643-G-A

14239924-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron variant
orthologous variants: 13215452-G-T

14240431-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: synonymous_variant, undefined
orthologous variants: 13216282-G-C

http://identifiers.org/hco/16/GRCh38#14240720-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 3_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#13216536-C-A

14240720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 3_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 13216536-C-T

http://identifiers.org/hco/16/GRCh38#14240790-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#13216583-A-C

14240819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 3_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 13216597-C-T

14240820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 13216598-A-G

14240845-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 13216626-T-C

14240935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 13216691-G-A

14240935-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 13216691-G-C

14240935-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 13216691-G-T

14241025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 13216738-G-A

14241025-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 13216738-G-C

14241025-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 13216738-G-T

14241131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 13216817-G-A

14241131-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 13216817-G-C

http://identifiers.org/hco/16/GRCh38#14241156-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#13216839-C-A

14241156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 13216839-C-T

http://identifiers.org/hco/16/GRCh38#14241166-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#13216849-C-A

14241166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 13216849-C-T

http://identifiers.org/hco/16/GRCh38#14241183-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#13216866-A-C

14241186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 13216869-G-A

14241186-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 13216869-G-T

14241202-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 13216885-G-T

14241203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 13216886-A-G

14241203-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 13216886-A-T

14241249-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 13216941-T-C

14241324-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 13217019-T-A

14241324-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 13217019-T-C

14241331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 13217026-G-A

14241331-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 13217026-G-T

14241367-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 13217044-G-T

http://identifiers.org/hco/16/GRCh38#14241614-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#13217236-A-C

14241614-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron variant
orthologous variants: 13217236-A-G

14245358-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron variant
orthologous variants: 13217784-T-C

14245426-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron variant
orthologous variants: 13217852-A-G

14245433-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron variant
orthologous variants: 13217858-T-C

14245497-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron variant
orthologous variants: 13217914-T-C

14245545-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: missense variant
orthologous variants: 13217955-A-G

14245577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: missense variant
orthologous variants: 13217978-G-A

14245755-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron variant
orthologous variants: 13218135-T-A

http://identifiers.org/hco/16/GRCh38#14245779-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#13218159-A-C

14245780-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron variant
orthologous variants: 13218160-T-A

14245781-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron variant
orthologous variants: 13218161-G-T

14246617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: missense variant
orthologous variants: 13218661-G-A

14246617-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: missense variant
orthologous variants: 13218661-G-T

http://identifiers.org/hco/16/GRCh38#14246874-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#13218918-C-A

14246874-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: missense variant
orthologous variants: 13218918-C-G

14246874-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: synonymous variant
orthologous variants: 13218918-C-T

14247093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: synonymous variant
orthologous variants: 13219134-G-A

14247147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: synonymous variant
orthologous variants: 13219191-G-A

14247147-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: missense variant
orthologous variants: 13219191-G-C

14247261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: synonymous variant
orthologous variants: 13219305-A-G

http://identifiers.org/hco/16/GRCh38#14247444-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#13219485-A-C

14247444-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 13219485-A-G

14247498-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 13219539-C-G

14247645-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 13219661-G-T

http://identifiers.org/hco/16/GRCh38#14247708-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#13219719-C-A

14247708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 13219719-C-T

http://identifiers.org/hco/16/GRCh38#14247955-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#13220022-A-C

14247955-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 13220022-A-G

14247980-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 13220051-A-G

http://identifiers.org/hco/16/GRCh38#14248273-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#13220267-C-A

14248273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 13220267-C-T

http://identifiers.org/hco/16/GRCh38#14248338-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#13220300-C-A

14248338-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 13220300-C-T

14248360-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 13220321-C-G

14248360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 13220321-C-T

14248365-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 13220327-A-G

http://identifiers.org/hco/16/GRCh38#14248386-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#13220357-C-A

14248489-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 13220461-T-C

14248620-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 13220568-G-T

http://identifiers.org/hco/16/GRCh38#14248653-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#13220599-A-C

http://identifiers.org/hco/16/GRCh38#14248828-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#13220930-A-C

14248955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 13221048-G-A

14249012-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 13221105-C-G

14249424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13221467-A-G

14251609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13222953-G-A

14251766-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13223057-A-G

http://identifiers.org/hco/16/GRCh38#14251918-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#13223166-C-A

14252255-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13223529-T-C

http://identifiers.org/hco/16/GRCh38#14252295-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#13223563-C-A

14257760-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13227169-G-C

14257970-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13227371-A-T

14258086-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13227466-T-A

14258086-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13227466-T-C

14258086-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13227466-T-G

http://identifiers.org/hco/16/GRCh38#14258186-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#13227565-C-A

14258186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 13227565-C-T

14258196-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 13227575-G-C

14258219-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 13227598-G-C

14258259-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 13227636-T-C

http://identifiers.org/hco/16/GRCh38#14258277-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#13227654-A-C

14258277-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 13227654-A-G

14260785-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 13229932-A-T

14260809-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 13229949-A-G

14261003-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 13230118-G-T

14261429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 13230544-G-A

14261429-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 13230544-G-C

14261481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 13230596-A-G

http://identifiers.org/hco/16/GRCh38#14261544-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#13230662-C-A

http://identifiers.org/hco/16/GRCh38#14261559-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#13230677-C-A

14261653-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 13230744-G-T

14261766-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 13230786-G-T

http://identifiers.org/hco/16/GRCh38#14261789-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#13230808-A-C

14262715-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 13231620-C-G

14262748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 13231653-G-A

14262748-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 13231653-G-T

http://identifiers.org/hco/16/GRCh38#14262945-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#13231835-C-A

14262945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 13231835-C-T

14263669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 13232345-G-A

14263692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 13232363-G-A

14263692-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 13232363-G-T

14263890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 13232517-G-A

14263890-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 13232517-G-T

14263949-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 13232584-A-G

14263995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 13232630-A-G

http://identifiers.org/hco/16/GRCh38#14264015-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#13232660-C-A

http://identifiers.org/hco/16/GRCh38#14264111-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#13232892-C-A

http://identifiers.org/hco/16/GRCh38#14264243-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#13233014-C-A

http://identifiers.org/hco/16/GRCh38#14264252-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#13233031-C-A

14264252-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 13233031-C-G

14264275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 13233054-T-C

14264289-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 13233068-T-C

14264290-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 13233069-A-G

14264334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 13233109-A-G

http://identifiers.org/hco/16/GRCh38#14264416-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#13233171-C-A

14264416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 13233171-C-T

14264464-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 13233214-G-C

14264587-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 13233298-A-G

14264717-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 13233385-T-C

14264718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 13233386-G-A

14264718-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 13233386-G-T

14264749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 13233392-G-A

14264749-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 13233392-G-T

14264778-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 13233421-T-C

http://identifiers.org/hco/16/GRCh38#14264788-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#13233435-A-C

14264788-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 13233435-A-T

14264807-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 13233447-A-G

http://identifiers.org/hco/16/GRCh38#14265080-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#13233649-C-A

14265141-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 13233699-G-C

14265141-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 13233699-G-T

http://identifiers.org/hco/16/GRCh38#14265196-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#13233747-C-A

14265309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 13233848-A-G

http://identifiers.org/hco/16/GRCh38#14265358-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#13233894-A-C

14265373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 13233909-C-T

14265512-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 13234049-T-G

14265617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 13234226-G-A

14265995-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 13234643-G-T

14266270-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 13234898-G-T

14266419-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 13235037-G-T

14266488-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 13235105-A-G

14266702-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29819
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 13235316-G-T