111540315-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: 5 prime UTR variant
orthologous variants: 50988740-T-C

http://identifiers.org/hco/11/GRCh38#111540331-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50988724-C-A

111540331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: 5 prime UTR variant
orthologous variants: 50988724-C-T

http://identifiers.org/hco/11/GRCh38#111540337-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50988718-A-C

111540337-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: intron variant
orthologous variants: 50988718-A-G

111540426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: intron variant
orthologous variants: 50988663-G-A

111540426-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: intron variant
orthologous variants: 50988663-G-T

111540455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: intron_variant, undefined
orthologous variants: 50988636-A-G

http://identifiers.org/hco/11/GRCh38#111540548-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50988554-A-C

111540548-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 50988554-A-G

111540630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 50988482-G-A

111540630-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 50988482-G-C

111540630-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 50988482-G-T

http://identifiers.org/hco/11/GRCh38#111540676-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50988435-C-A

111540676-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 50988435-C-G

111540676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 50988435-C-T

111540819-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 50988291-T-A

http://identifiers.org/hco/11/GRCh38#111540850-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50988262-C-A

111540850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 50988262-C-T

111540965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50988142-G-A

111540976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50988131-G-A

http://identifiers.org/hco/11/GRCh38#111541044-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#50988045-A-C

111541173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50987929-C-T

111541195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50987908-G-A

111541195-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50987908-G-T

http://identifiers.org/hco/11/GRCh38#111541233-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50987870-C-A

111541233-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50987870-C-G

111541233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50987870-C-T

http://identifiers.org/hco/11/GRCh38#111541249-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50987854-C-A

111541249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50987854-C-T

111541305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50987849-G-A

111541305-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50987849-G-T

http://identifiers.org/hco/11/GRCh38#111541306-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50987848-C-A

111541306-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50987848-C-G

111541306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50987848-C-T

111541459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 50987745-G-A

111541459-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 50987745-G-C

111541537-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 50987669-C-T

111541788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 50987394-G-A

http://identifiers.org/hco/11/GRCh38#111541837-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50987342-C-A

111542626-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50986710-T-G

111542833-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50986522-T-A

111542847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50986511-G-A

111542875-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50986483-A-T

111542888-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50986471-A-T

http://identifiers.org/hco/11/GRCh38#111543034-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50986325-A-C

111543145-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50986221-G-T

111543704-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50985714-A-T

111543883-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50985539-T-C

111543943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 50985423-G-A

111543943-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 50985423-G-T

111544249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50985117-C-T

111544254-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50985112-T-G

111544274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50985092-G-A

http://identifiers.org/hco/11/GRCh38#111544276-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50985090-C-A

111544276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50985090-C-T

111544291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50985075-G-A

111544291-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50985075-G-T

111544307-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50985059-G-T

111544375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50984991-T-C

111544953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50984346-T-C

111545432-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50983712-G-T

111545493-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50983640-A-G

111545591-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50983569-G-C

111547088-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50982075-C-T

111547153-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50982024-A-G

111547166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50982014-C-T

http://identifiers.org/hco/11/GRCh38#111547172-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50982008-A-C

111547173-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50982007-C-G

111547218-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50981968-G-T

111547289-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50981900-A-G

111547332-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50981857-G-C

111547339-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50981850-A-G

http://identifiers.org/hco/11/GRCh38#111547342-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50981825-C-A

http://identifiers.org/hco/11/GRCh38#111547489-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50981694-C-A

111547489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50981694-C-T

111547825-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50981396-T-A

111548125-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50980988-G-C

111548175-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50980953-G-T

111548204-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50980924-A-G

111548567-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50980498-A-G

111548829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50980236-G-A

111548989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50980140-A-G

111549091-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50980037-C-G

111549154-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 50979974-T-C

111549176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50979952-G-A

111549191-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50979940-T-A

111549191-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50979940-T-C

111549280-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50979852-A-G

http://identifiers.org/hco/11/GRCh38#111549532-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50979584-C-A

111549532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50979584-C-T

111549576-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50979536-A-T

111549691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 50979421-G-A

111549768-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 50979344-T-C

111549799-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50979314-T-A

111549815-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 50979298-A-G

111549827-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50979283-T-A

111549827-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50979283-T-C

111549928-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50979182-A-G

111550025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50979087-T-C

111550205-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50978924-T-C

111550389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50978731-G-A

111550532-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50978586-T-C

111550706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50978411-C-T

111551274-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50977879-C-G

111551344-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 50977820-A-T

111551442-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50977738-T-C

111551442-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50977738-T-G

111551527-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50977686-G-T

111551614-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50977598-T-G

111551880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50977317-G-A

111551948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50977257-G-A

111551962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50977238-C-T

111552078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50977166-T-C

111552166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50977099-C-T

111552348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50976961-A-G

111552390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50976920-G-A

111552588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50976733-T-C

111552589-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50976732-G-A

111552614-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50976705-A-G

111552649-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50976666-T-C

111552661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50976654-C-T

http://identifiers.org/hco/11/GRCh38#111552678-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50976637-C-A

111552736-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50976591-T-C

111552811-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50976498-C-G

111552916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50976411-G-A

111552976-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50976363-A-T

111552992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50976348-C-T

111553710-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50976208-A-G

http://identifiers.org/hco/11/GRCh38#111553771-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50976137-A-C

111554121-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50975864-A-G

111554323-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50975668-T-A

111554323-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50975668-T-C

111554394-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50974727-A-G

111554582-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, missense_variant, stop_lost
orthologous variants: 50974546-G-C

111554582-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, missense_variant, stop_lost
orthologous variants: 50974546-G-T

111554618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50974510-G-A

http://identifiers.org/hco/11/GRCh38#111554629-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50974499-C-A

111554629-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50974499-C-T

111554631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50974497-G-A

111554631-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50974497-G-C

111554631-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50974497-G-T

111554634-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50974494-T-C

111554638-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50974490-A-G

http://identifiers.org/hco/11/GRCh38#111554640-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50974488-C-A

111554640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50974488-C-T

http://identifiers.org/hco/11/GRCh38#111554690-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50974442-C-A

111554690-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50974442-C-G

111554694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50974438-A-G

111554701-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50974431-G-A

111554701-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50974431-G-T

http://identifiers.org/hco/11/GRCh38#111554740-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50974392-A-C

111554740-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50974392-A-T

111554770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50974373-C-T

111554778-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50974365-A-G

111554920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50974183-G-A

111554977-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50974126-T-C

http://identifiers.org/hco/11/GRCh38#111555110-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50973665-C-A

http://identifiers.org/hco/11/GRCh38#111555126-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50973649-C-A

111555126-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50973649-C-G

111555136-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50973639-A-G

111555159-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50973616-T-A

111555340-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50973445-T-C

111555397-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50973389-T-C

111555457-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50973329-A-G

111555486-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50973300-A-G

111555613-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50973165-A-G

111555674-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50973100-G-T

111555811-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50972964-A-G

http://identifiers.org/hco/11/GRCh38#111556086-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50972687-A-C

111556133-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50972644-A-G

http://identifiers.org/hco/11/GRCh38#111556525-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50971873-C-A

111556532-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50971866-A-G

111556583-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50971801-C-G

111556583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50971801-C-T

111556680-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50971696-A-T

111557030-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50971339-A-G

111557348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50971057-C-T

111557402-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50971022-T-A

111557402-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50971022-T-C

111557708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50970700-C-T

111557842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50970549-T-C

111558187-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50970210-A-T

http://identifiers.org/hco/11/GRCh38#111558310-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50970102-A-C

111558434-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50969984-A-T

111558439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50969981-G-A

111558978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50969609-G-A

111559233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50969451-G-A

111559233-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50969451-G-C

111559778-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50969221-T-C

111560000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50969041-G-A

111560000-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50969041-G-T

111560102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 50968947-G-A

111560279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 50968770-C-T

111560400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 50968649-A-G

111560557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 50968504-G-A

http://identifiers.org/hco/11/GRCh38#111560602-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50968463-C-A

111560602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 50968463-C-T

111560661-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 50968404-T-C

http://identifiers.org/hco/11/GRCh38#111560686-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50968378-C-A

111560693-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 50968371-A-G

http://identifiers.org/hco/11/GRCh38#111560711-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50968355-A-C

111560711-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 50968355-A-T

http://identifiers.org/hco/11/GRCh38#111560752-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50968314-C-A

111560764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 50968301-G-A

111560790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 50968275-G-A

111560790-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 50968275-G-T

http://identifiers.org/hco/11/GRCh38#111560796-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50968268-C-A

111560875-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 50968182-T-A

111560875-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 50968182-T-G

http://identifiers.org/hco/11/GRCh38#111560886-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50968170-A-C

111560886-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 50968170-A-G

111560886-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 50968170-A-T

111560969-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 50968075-T-C

111560969-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29471
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 50968075-T-G