http://identifiers.org/hco/7/GRCh38#49773688-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#11064107-C-A

49773688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: 5 prime UTR variant
orthologous variants: 11064107-C-T

49773689-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: 5 prime UTR variant
orthologous variants: 11064108-G-C

49773689-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: 5 prime UTR variant
orthologous variants: 11064108-G-T

http://identifiers.org/hco/7/GRCh38#49773704-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#11064123-C-A

49773704-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: 5 prime UTR variant
orthologous variants: 11064123-C-T

49773820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: 5 prime UTR variant
orthologous variants: 11064237-T-C

49773824-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: 5 prime UTR variant
orthologous variants: 11064241-A-G

49773843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: 5 prime UTR variant
orthologous variants: 11064262-G-A

49773843-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: 5 prime UTR variant
orthologous variants: 11064262-G-T

49773851-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: 5 prime UTR variant
orthologous variants: 11064270-G-T

49773963-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: 5 prime UTR variant
orthologous variants: 11064380-G-T

http://identifiers.org/hco/7/GRCh38#49774042-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#11064460-C-A

49774042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: 5 prime UTR variant
orthologous variants: 11064460-C-T

http://identifiers.org/hco/7/GRCh38#49774050-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#11064468-C-A

49774088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: 5 prime UTR variant
orthologous variants: 11064484-G-A

http://identifiers.org/hco/7/GRCh38#49774175-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#11064569-C-A

49774175-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron variant
orthologous variants: 11064569-C-G

49774175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron variant
orthologous variants: 11064569-C-T

http://identifiers.org/hco/7/GRCh38#49774185-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#11064579-C-A

49774185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron variant
orthologous variants: 11064579-C-T

49774187-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron variant
orthologous variants: 11064581-A-G

49774193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron variant
orthologous variants: 11064587-G-A

49774193-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron variant
orthologous variants: 11064587-G-T

49774280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron variant
orthologous variants: 11064675-G-A

49774489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron variant
orthologous variants: 11064885-G-A

49774501-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron variant
orthologous variants: 11064896-G-C

49774613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron variant
orthologous variants: 11065021-G-A

49774622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron variant
orthologous variants: 11065030-G-A

49774622-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron variant
orthologous variants: 11065030-G-C

49774638-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron variant
orthologous variants: 11065077-A-G

49774656-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron variant
orthologous variants: 11065095-C-G

49774656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron variant
orthologous variants: 11065095-C-T

49774691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron variant
orthologous variants: 11065129-C-T

49774746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron variant
orthologous variants: 11065172-G-A

49774804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron variant
orthologous variants: 11065224-C-T

http://identifiers.org/hco/7/GRCh38#49774812-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#11065232-C-A

49775033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron variant
orthologous variants: 11065496-C-T

49775063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron variant
orthologous variants: 11065527-C-T

49775134-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron variant
orthologous variants: 11065597-T-C

49775190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron variant
orthologous variants: 11065651-G-A

49775190-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron variant
orthologous variants: 11065651-G-T

49775224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron variant
orthologous variants: 11065686-G-A

49775224-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron variant
orthologous variants: 11065686-G-C

49775224-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron variant
orthologous variants: 11065686-G-T

49775236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron variant
orthologous variants: 11065698-G-A

49775236-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron variant
orthologous variants: 11065698-G-C

49775236-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron variant
orthologous variants: 11065698-G-T

http://identifiers.org/hco/7/GRCh38#49775307-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#11065785-C-A

49775307-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron variant
orthologous variants: 11065785-C-G

49775307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron variant
orthologous variants: 11065785-C-T

49775337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 11065815-G-A

49775337-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 11065815-G-C

49775337-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 11065815-G-T

49775588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 11066066-C-T

49775710-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 11066188-A-G

49775710-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 11066188-A-T

49775771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 11066249-G-A

49775771-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 11066249-G-T

49775966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 11066441-G-A

49775966-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 11066441-G-C

49775966-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 11066441-G-T

http://identifiers.org/hco/7/GRCh38#49776022-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#11066497-A-C

49776022-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 11066497-A-G

http://identifiers.org/hco/7/GRCh38#49776041-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#11066516-C-A

49776041-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 11066516-C-G

49776041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 11066516-C-T

49776233-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11066724-T-G

49776241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11066732-G-A

49776241-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11066732-G-C

49776241-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11066732-G-T

49776276-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11066764-A-G

49776290-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11066775-G-C

49776295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11066780-G-A

49776492-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11066966-A-G

49776840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11067282-G-A

49777040-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11067476-A-G

49777149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11067579-G-A

49777334-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11067745-A-T

49777421-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11067822-G-T

49777911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11068171-G-A

49777911-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11068171-G-C

http://identifiers.org/hco/7/GRCh38#49777996-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#11068256-C-A

49777999-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11068259-G-T

49778174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11068452-G-A

49778227-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11068502-A-G

49778286-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11068559-G-T

49778364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11068918-C-T

49778591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11069137-C-T

49778593-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11069139-A-G

49778600-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11069146-T-A

49778969-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11069404-G-T

49779139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11069541-C-T

49779186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11069599-C-T

49779240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11069642-C-T

49779629-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11069971-G-C

49779655-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11069996-G-C

49779797-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11070113-G-A

49779797-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11070113-G-T

49780242-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11070636-C-G

49780603-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11070980-A-G

49780692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11071065-A-G

http://identifiers.org/hco/7/GRCh38#49780715-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#11071085-A-C

49780818-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11071185-A-T

49780825-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11071192-A-T

http://identifiers.org/hco/7/GRCh38#49780829-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#11071197-A-C

49781788-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11071670-T-C

49781798-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11071680-A-G

49781927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11071801-G-A

49781986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11071855-C-T

http://identifiers.org/hco/7/GRCh38#49782021-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#11071880-C-A

49782393-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11072182-C-G

49782488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11072260-C-T

49783073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11072511-C-T

49783076-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11072514-A-G

49783204-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11072637-A-G

49783315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11072746-C-T

49783419-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11072866-T-C

49783438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11072885-G-A

49783438-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11072885-G-C

49783501-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11072944-C-G

49783579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11073018-C-T

49783941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11073202-G-A

http://identifiers.org/hco/7/GRCh38#49784054-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#11073284-C-A

49784117-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11073362-T-C

49787057-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11078651-A-G

49787074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11078667-A-G

49787285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11078839-C-T

49787352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11078896-A-G

49787756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11079235-C-T

49787795-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11079273-C-G

http://identifiers.org/hco/7/GRCh38#49787849-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#11079321-C-A

49787849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11079321-C-T

49788028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11079495-G-A

49788219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11079673-T-C

49788337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11079755-G-A

49788344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11079762-G-A

49788353-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11079771-T-C

49789435-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11079971-A-G

49789636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11080160-G-A

49789676-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11080182-T-G

49789725-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11080286-A-G

49789726-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11080287-C-G

49789840-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11080393-A-G

49789951-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11080715-G-C

49789951-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11080715-G-T

49790081-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11080837-G-C

49790346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11081066-G-A

49790508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11081233-C-T

49791038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11081667-C-T

49791105-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 11081725-C-G

49791107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 11081727-C-T

49791196-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 11081808-T-C

49791321-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 11081928-G-C

49791538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11082156-G-A

49791816-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11082889-T-C

49791936-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11083004-G-T

49792007-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11083074-G-C

49792411-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11083560-G-T

49792451-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11083595-G-T

49792649-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11083780-C-G

49792759-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11083910-G-T

49792768-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11083919-A-G

49792819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11083952-G-A

49792828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11083961-G-A

49792878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11084016-G-A

49792918-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11084101-A-G

49792924-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11084107-A-G

49792930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11084114-C-T

49792931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11084115-C-T

49793044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11084284-G-A

http://identifiers.org/hco/7/GRCh38#49793101-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#11084340-A-C

49793101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11084340-A-G

49793143-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11084381-T-G

49793174-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11084412-T-C

49793205-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11089166-A-G

49793239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11089191-G-A

49793332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11089291-C-T

49793417-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11089373-C-G

49793467-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11089410-G-T

49793553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11089495-A-G

49793689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11089635-T-C

49793847-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11089735-T-A

49793890-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11089778-T-C

http://identifiers.org/hco/7/GRCh38#49793936-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#11089825-C-A

49793936-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11089825-C-G

49794166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11090057-C-T

49794167-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11090058-T-A

49794390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11090933-G-A

49794390-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11090933-G-T

49794444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11090966-C-T

49794516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11091011-C-T

49794598-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11091049-T-G

49794599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11091050-G-A

49796143-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11099244-A-T

49796260-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11099348-T-A

49796260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11099348-T-C

49796307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11099395-C-T

49796313-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11099401-A-T

http://identifiers.org/hco/7/GRCh38#49796334-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#11099422-C-A

49796375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11099463-C-T

49796478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11099563-G-A

49796500-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11099597-T-G

49796979-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11100289-G-T

http://identifiers.org/hco/7/GRCh38#49797070-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#11100379-A-C

49797070-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11100379-A-G

49797317-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11099379-T-C

49797427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11100525-A-G

49797427-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11100525-A-T

49797462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11100559-G-A

49797530-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11100631-A-G

49797584-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11100688-G-C

49797584-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11100688-G-T

49797640-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11101267-T-C

http://identifiers.org/hco/7/GRCh38#49800668-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#11102973-C-A

49800968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11103184-C-T

49802862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11104316-G-A

49802879-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11104333-A-T

http://identifiers.org/hco/7/GRCh38#49802946-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#11104390-C-A

49802946-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11104390-C-G

49802947-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11104391-T-A

http://identifiers.org/hco/7/GRCh38#49802983-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#11104421-C-A

49802983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11104421-C-T

49802989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11104427-G-A

49802989-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11104427-G-C

49803183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11104626-C-T

49803573-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11104976-G-T

49803577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11104980-C-T

49803586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11104988-G-A

49803636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11105056-G-A

49803766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11105157-G-A

49803766-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11105157-G-C

49803775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11105166-G-A

49803969-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11105325-T-C

49804287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11106229-G-A

49804352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11106309-G-A

49804352-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11106309-G-C

49804352-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11106309-G-T

49804419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11106377-C-T

http://identifiers.org/hco/7/GRCh38#49804450-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#11106406-A-C

49804711-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11106677-T-C

49804835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11106814-T-C

49805508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11107998-G-A

49805652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11108126-C-T

49805784-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11108260-G-C

http://identifiers.org/hco/7/GRCh38#49806031-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#11108503-A-C

http://identifiers.org/hco/7/GRCh38#49806220-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#11108666-C-A

49806220-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11108666-C-G

49806246-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11108692-A-G

49806816-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11109183-T-C

http://identifiers.org/hco/7/GRCh38#49806838-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#11109204-C-A

49806958-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11109310-A-T

49806991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11109362-G-A

49806991-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11109362-G-C

49807212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11109770-G-A

49807296-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11109857-C-G

49807305-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11109866-A-G

49807312-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11109874-A-G

49807341-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11109898-T-C

http://identifiers.org/hco/7/GRCh38#49807462-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#11110002-C-A

49807493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11110018-C-T

49807512-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11110036-T-C

49807552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11110078-G-A

49807577-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11110103-T-C

49807678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11110222-A-G

49807887-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11110438-A-T

49808074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11110571-G-A

49808074-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11110571-G-T

49808080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11110577-G-A

49810324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11116025-G-A

49810370-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11116079-T-C

49810509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11116228-G-A

49810535-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11116254-T-A

49810600-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11116309-A-T

49810927-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11116698-T-C

49811053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11116856-C-T

49811163-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11116972-A-T

49811699-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11117434-A-G

49811852-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11117584-T-C

49811923-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11117749-T-C

49811983-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11117807-C-G

49812004-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11117828-T-G

http://identifiers.org/hco/7/GRCh38#49812043-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#11117855-A-C

49812335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11118329-C-T

49813036-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11118798-G-C

http://identifiers.org/hco/7/GRCh38#49813257-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#11119007-A-C

http://identifiers.org/hco/7/GRCh38#49813581-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#11119307-C-A

http://identifiers.org/hco/7/GRCh38#49813954-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#11119621-C-A

49813954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11119621-C-T

49814094-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11119733-G-A

49814258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11119890-C-T

http://identifiers.org/hco/7/GRCh38#49814344-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#11119983-C-A

49814750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11121078-C-T

49815447-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11121767-G-T

49815642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11121953-A-G

49815714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11122023-C-T

49815802-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11122091-T-A

49815822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11122111-G-A

49815858-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11122147-A-G

49816929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11124456-G-A

49817075-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11124667-T-C

49817171-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11124746-A-T

49817447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11125015-C-T

49817491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11125059-G-A

49817599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11125162-C-T

49817680-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11125240-A-G

49817781-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11125347-T-C

49817853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11125419-T-C

http://identifiers.org/hco/7/GRCh38#49817949-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#11125519-C-A

49817988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11125554-T-C

49818050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11125618-C-T

49819456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11126140-C-T

http://identifiers.org/hco/7/GRCh38#49819458-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#11126142-A-C

49819470-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11126153-A-G

49819623-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11126294-G-C

49819689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11126356-G-A

49820067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11126714-C-T

49820155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11126779-G-A

49820310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11126915-C-T

49820311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11126917-G-A

http://identifiers.org/hco/7/GRCh38#49820665-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#11127429-A-C

http://identifiers.org/hco/7/GRCh38#49820726-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#11127493-C-A

49820758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11127521-G-A

49820779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11127542-A-G

http://identifiers.org/hco/7/GRCh38#49827600-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#11143149-C-A

49827600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11143149-C-T

49827750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11143297-G-A

49828569-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11144760-G-T

49828648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11144822-G-A

49828648-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11144822-G-T

49828917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11145074-C-T

49829004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11145147-G-A

49829121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11145266-G-A

http://identifiers.org/hco/7/GRCh38#49829175-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#11145319-A-C

49829175-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11145319-A-G

49829260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11145410-C-T

49829290-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11145444-T-A

49829359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11145505-G-A

49829359-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11145505-G-T

49829426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11145571-C-T

http://identifiers.org/hco/7/GRCh38#49829459-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#11145604-C-A

49829459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11145604-C-T

49829510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11145647-C-T

http://identifiers.org/hco/7/GRCh38#49829535-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#11145684-A-C

49829611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11145760-G-A

http://identifiers.org/hco/7/GRCh38#49829634-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#11145781-A-C

49829752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11145924-C-T

49829838-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11146003-T-C

49830133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11146312-C-T

49830181-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11146353-T-A

49830470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11146557-G-A

49834518-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11150657-T-A

49834607-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11150747-T-C

49834610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11150750-A-G

49834626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11150766-G-A

49834785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11150930-G-A

49836058-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11151166-T-C

49836082-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11151215-G-T

49836244-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11151355-G-T

http://identifiers.org/hco/7/GRCh38#49836287-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#11151395-C-A

49836763-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11151512-A-G

49836763-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11151512-A-T

49836878-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11151598-T-C

49836967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11151679-G-A

49837148-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11151860-A-G

49837183-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11151895-G-T

49837397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11152127-C-T

49837418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11152148-A-G

49837468-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11152195-T-A

49837497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11152212-G-A

49837540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11152252-G-A

49837540-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11152252-G-C

http://identifiers.org/hco/7/GRCh38#49837688-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#11152513-A-C

49837859-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11152679-A-G

49838134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11152936-G-A

49838134-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11152936-G-C

49838138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11152940-G-A

49838138-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11152940-G-C

49838283-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11153072-G-T

49838369-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11153160-T-A

49838742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11153521-G-A

49838743-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11153522-G-C

49838797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11153566-C-T

49838813-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11153578-A-G

49838815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11153580-G-A

49838952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11153748-C-T

49838954-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11153750-G-C

49840098-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11159298-C-G

49840098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11159298-C-T

49840113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11159313-A-G

49840118-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11159318-C-T

49840176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11159357-A-G

49840325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11159487-G-A

49840325-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11159487-G-C

49840337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11159499-C-T

49840410-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11159723-T-C

49840638-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11160034-G-C

49840811-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11160213-T-G

49840882-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11160279-C-G

49840937-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11160334-A-G

49841100-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11160474-A-G

49841143-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11160513-C-G

49841348-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11160687-G-T

49841374-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11160712-G-T

49841399-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11160748-A-T

49841409-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11160770-T-G

http://identifiers.org/hco/7/GRCh38#49842172-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#11161896-C-A

49842367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11162188-G-A

49842525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11162393-C-T

49842794-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11162688-T-C

http://identifiers.org/hco/7/GRCh38#49843262-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#11162874-C-A

49843262-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11162874-C-G

49843262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11162874-C-T

49843299-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11162901-T-G

49843385-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11162987-C-G

http://identifiers.org/hco/7/GRCh38#49843404-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#11163006-A-C

49843404-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11163006-A-G

49843606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11163209-T-C

49843708-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11165716-T-C

49843745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11165679-G-A

http://identifiers.org/hco/7/GRCh38#49844000-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#11165431-A-C

49844096-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11165172-A-T

http://identifiers.org/hco/7/GRCh38#49844100-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#11165165-C-A

49844100-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11165165-C-G

49844100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11165165-C-T

49844121-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11165145-A-G

49844159-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11165113-A-G

49844309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11164970-A-G

http://identifiers.org/hco/7/GRCh38#49844375-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#11164908-A-C

49844375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11164908-A-G

49844396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11164900-C-T

49844451-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11164849-G-C

49844659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11164679-G-A

49844678-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11164660-G-C

49845412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11164538-C-T

49845514-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11164445-A-T

49845565-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11164381-T-C

49845882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11163681-C-T

http://identifiers.org/hco/7/GRCh38#49846128-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#11163419-A-C

49846224-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11163325-T-C

49846291-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11163265-T-C

49846291-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11163265-T-G

49846627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11165844-G-A

49846670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11165887-G-A

49846708-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11165925-A-G

49846848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11166058-C-T

49846865-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11166076-T-C

49847071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11166265-T-C

49847158-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11166363-A-G

49847209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11166476-C-T

49847699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11167136-C-T

49847711-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11167148-G-T

49847721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11167158-C-T

49847772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11167210-G-A

49847856-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11167288-G-C

49848040-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11167439-A-G

49848204-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11167595-T-C

49848330-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11167689-T-C

http://identifiers.org/hco/7/GRCh38#49848685-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#11168257-C-A

49848685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11168257-C-T

49848717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11168363-G-A

49848730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11168384-C-T

49848753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11168404-A-G

49848820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11168468-C-T

49848889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11168533-G-A

49849150-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11168908-C-G

49849150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11168908-C-T

49849209-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11168946-A-G

49849312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11169022-G-A

49849394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11169093-C-T

http://identifiers.org/hco/7/GRCh38#49849542-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#11169228-C-A

49849676-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11169346-G-C

49849705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11169376-G-A

49849913-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11169552-T-A

49849936-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11169575-T-G

49849997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11169616-G-A

http://identifiers.org/hco/7/GRCh38#49850070-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#11169682-A-C

49850070-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11169682-A-G

49850440-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11169857-G-T

49850454-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11169871-G-T

49850505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 11169921-G-A

49850505-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11169921-G-T

49850538-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11169950-C-T

49850568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11169986-G-A

49850569-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11169991-T-C

49850663-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11170083-A-G

49850683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11170094-G-A

49850783-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11170185-T-C

49851054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11170404-G-A

49851148-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11170491-T-A

49851866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11171591-A-G

49851877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11171602-C-T

49851881-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11171606-A-G

49851920-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11171643-G-C

49852158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11171883-C-T

49852258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11171951-G-A

49852275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11171966-T-C

49852369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11172049-G-A

49852397-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11172057-A-G

49852413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11172073-G-A

49852417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11172077-G-A

49852417-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11172077-G-C

49852418-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11172078-G-C

49852448-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11172101-T-C

49852448-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11172101-T-G

49852477-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11172130-A-G

49852850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11173377-C-T

49852972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11173491-C-T

49853224-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11173761-C-G

49853224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11173761-C-T

49866054-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11177951-T-G

49866431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11178307-C-T

49866532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11178408-G-A

49866586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11178431-G-A

49866586-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11178431-G-C

49866590-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11178435-A-G

49866779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11178591-G-A

49867081-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11178850-T-C

49867179-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11178928-T-A

49867187-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11178936-A-G

49867187-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11178936-A-T

49868137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11179872-G-A

49868169-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11179904-T-C

49868327-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11180054-A-G

49868445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11180178-C-T

49869340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11180431-C-T

49869438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11180505-C-T

49869479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11180526-T-C

http://identifiers.org/hco/7/GRCh38#49869557-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#11180604-C-A

49869625-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11180720-G-C

http://identifiers.org/hco/7/GRCh38#49869661-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#11180775-A-C

49869661-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11180775-A-G

49869667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11180798-C-T

49869748-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11180943-A-G

49869832-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11181030-A-G

49869832-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11181030-A-T

49869855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11181054-G-A

49869855-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11181054-G-T

49869858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11181057-C-T

49871357-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11187208-T-C

49871666-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11187508-A-T

49872093-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11187791-T-G

49875439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11191327-A-G

49875480-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11191368-A-G

49875613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11191494-C-T

49875840-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11192003-T-G

http://identifiers.org/hco/7/GRCh38#49876110-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#11192250-A-C

49876188-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11192335-G-C

49876542-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11192678-A-G

49876634-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11192763-A-G

49876647-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11192776-T-C

49877064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11193198-A-G

49877591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11193377-T-C

49877670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11193447-G-A

49878618-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11194125-T-C

49878659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11194170-G-A

49878706-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11194207-A-G

49878706-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11194207-A-T

http://identifiers.org/hco/7/GRCh38#49878723-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#11194222-C-A

49878723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11194222-C-T

http://identifiers.org/hco/7/GRCh38#49879535-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#11194875-A-C

49879535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11194875-A-G

49879535-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11194875-A-T

http://identifiers.org/hco/7/GRCh38#49879759-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#11194915-C-A

49879789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11194945-A-G

49881434-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11195371-T-C

49881585-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11195526-C-G

49881831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11195765-G-A

49882253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11196228-G-A

http://identifiers.org/hco/7/GRCh38#49882324-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#11196289-C-A

49882324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11196289-C-T

49882357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11196325-A-G

49882450-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11196389-A-G

49882524-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11196464-C-T

49882569-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11196508-T-A

49882569-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11196508-T-G

49882630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11196586-G-A

49882690-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11196646-T-G

49910592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11210621-G-A

49910776-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11210803-A-G

49910845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11210864-A-G

49910907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11210913-C-T

49910927-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11210930-A-G

49910976-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11210969-T-A

49911081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11211066-C-T

http://identifiers.org/hco/7/GRCh38#49911526-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#11211216-C-A

49911985-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11211321-T-A

49911985-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11211321-T-C

49912161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 11211496-G-A

49912589-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11211902-A-G

49912589-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11211902-A-T

49912618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11211940-G-A

49912618-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11211940-G-C

49912618-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11211940-G-T

49912623-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11211945-A-G

49912638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11211960-G-A

49912638-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11211960-G-C

49912638-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11211960-G-T

http://identifiers.org/hco/7/GRCh38#49912639-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#11211961-A-C

49912639-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11211961-A-G

49912639-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11211961-A-T

49912640-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11211962-T-A

49912640-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11211962-T-C

49912640-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11211962-T-G

http://identifiers.org/hco/7/GRCh38#49912644-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#11211966-A-C

49912644-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11211966-A-G

49912644-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11211966-A-T

49912654-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11211976-G-T

49912769-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11212078-C-T

49912917-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11212209-G-T

49913139-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11212426-G-C

49913285-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11212561-G-T

49913326-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11212594-G-C

49913625-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11212834-G-T

http://identifiers.org/hco/7/GRCh38#49913698-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#11212912-C-A

http://identifiers.org/hco/7/GRCh38#49914035-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#11213230-C-A

49914109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11213307-G-A

49914158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11213364-C-T

49914358-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11213578-G-T

http://identifiers.org/hco/7/GRCh38#49914364-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#11213584-A-C

http://identifiers.org/hco/7/GRCh38#49914426-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#11213638-C-A

49914426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11213638-C-T

49914548-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11213703-T-C

49914548-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11213703-T-G

49914749-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11213878-G-C

49914749-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11213878-G-T

49914854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11213955-T-C

http://identifiers.org/hco/7/GRCh38#49915113-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#11214164-A-C

49915120-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11214171-G-C

49915120-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11214171-G-T

49915121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11214172-G-A

http://identifiers.org/hco/7/GRCh38#49915208-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#11214252-C-A

49915238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11214285-C-T

49915565-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11214594-G-C

49915812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11214824-G-A

49915812-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11214824-G-T

http://identifiers.org/hco/7/GRCh38#49916085-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#11215065-C-A

49916161-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11215136-T-G

49916190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11215165-G-A

49916190-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11215165-G-T

49916326-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11215278-G-T

http://identifiers.org/hco/7/GRCh38#49916343-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#11215294-C-A

49916474-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11215828-G-C

49916556-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11216099-T-C

49916664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11216204-T-C

http://identifiers.org/hco/7/GRCh38#49916792-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#11216311-C-A

49916792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11216311-C-T

http://identifiers.org/hco/7/GRCh38#49916801-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#11216320-A-C

49916962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11216468-G-A

49916962-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11216468-G-C

49917340-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11216855-T-C

49917430-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11216942-A-G

http://identifiers.org/hco/7/GRCh38#49917559-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#11217046-C-A

49917620-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11217099-T-C

49918456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11217624-C-T

49919066-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11218345-A-G

49919138-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11218421-G-T

49919158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11218441-C-T

http://identifiers.org/hco/7/GRCh38#49919213-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#11218507-C-A

49919221-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11218515-T-G

49919234-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11218528-T-C

49919304-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11218595-A-G

49919304-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11218595-A-T

49919452-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11218742-A-G

49919452-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11218742-A-T

49919604-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11218853-A-T

49919607-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11218858-A-T

http://identifiers.org/hco/7/GRCh38#49919673-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#11218921-C-A

49919688-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11218946-T-C

49919709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11218967-G-A

49919746-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11218999-A-G

49919789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11219037-A-G

49919930-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11219160-A-T

49920035-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11219267-T-C

http://identifiers.org/hco/7/GRCh38#49920073-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#11219301-C-A

49920119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11219339-G-A

49920139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11219359-G-A

49920139-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11219359-G-T

49920269-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11219488-G-T

http://identifiers.org/hco/7/GRCh38#49921308-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#11219553-C-A

49921308-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11219553-C-G

49921576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11219750-C-T

http://identifiers.org/hco/7/GRCh38#49921691-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#11219864-A-C

49921895-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11220028-G-C

http://identifiers.org/hco/7/GRCh38#49922064-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#11220173-A-C

http://identifiers.org/hco/7/GRCh38#49922181-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30200
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#11220297-C-A