180100797-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: 3 prime UTR variant
orthologous variants: 49871039-G-T

180100869-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 49870963-T-C

http://identifiers.org/hco/5/GRCh38#180100943-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49870891-A-C

180100943-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 49870891-A-G

180101004-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 49870833-G-T

http://identifiers.org/hco/5/GRCh38#180101066-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49870770-C-A

180101066-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 49870770-C-G

180101066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 49870770-C-T

http://identifiers.org/hco/5/GRCh38#180101137-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49870700-A-C

180101137-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 49870700-A-G

http://identifiers.org/hco/5/GRCh38#180101144-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49870693-C-A

180101144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 49870693-C-T

180101198-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 49870640-T-G

180101288-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 49870548-A-T

180101302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 49870532-G-A

180101302-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 49870532-G-T

180101339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 49870495-G-A

180101339-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 49870495-G-C

180101339-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 49870495-G-T

180101343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 49870491-G-A

180101343-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 49870491-G-T

180101523-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 49870322-G-C

180101523-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 49870322-G-T

180101545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49870300-G-A

180101552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49870290-G-A

180101569-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49870278-C-G

180101612-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49870240-T-C

180101640-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49870223-C-G

180101641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49870222-A-G

180101712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49870161-C-T

180101801-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49869549-T-C

180101928-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49869413-G-T

180101932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49869409-G-A

180101932-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49869409-G-C

180101951-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49869391-A-G

http://identifiers.org/hco/5/GRCh38#180101968-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49869375-C-A

180101968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49869375-C-T

http://identifiers.org/hco/5/GRCh38#180101969-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49869374-C-A

180101969-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49869374-C-G

180101969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49869374-C-T

180101971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49869372-G-A

180101978-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49869365-A-G

180102000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49869343-G-A

180102000-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49869343-G-T

180102139-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 49869237-A-G

180111165-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49866870-G-C

180111172-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49866863-G-C

180111206-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49866828-G-T

180111211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49866823-C-T

180111212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49866822-G-A

180111232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49866803-G-A

180111232-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49866803-G-C

180111234-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49866801-G-C

180111307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49866714-G-A

180111307-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49866714-G-T

http://identifiers.org/hco/5/GRCh38#180111327-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49866693-C-A

180111327-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49866693-C-G

http://identifiers.org/hco/5/GRCh38#180111456-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49866576-C-A

180111501-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 49866531-C-G

180112189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49864214-G-A

180112428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49864005-G-A

180112462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49863978-C-T

180113925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49863475-C-T

http://identifiers.org/hco/5/GRCh38#180114229-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49863198-C-A

180114229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49863198-C-T

180114316-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49863116-A-G

http://identifiers.org/hco/5/GRCh38#180114335-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49863096-C-A

180114335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49863096-C-T

180114356-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49863072-A-G

180114356-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49863072-A-T

http://identifiers.org/hco/5/GRCh38#180114385-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49863043-C-A

180114393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49862345-G-A

180114393-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49862345-G-T

http://identifiers.org/hco/5/GRCh38#180114425-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49862314-C-A

180114425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49862314-C-T

180116911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 49861826-C-T

180116912-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 49861825-A-G

180116950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49861789-C-T

180116962-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49861773-T-G

180117107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49861640-C-T

http://identifiers.org/hco/5/GRCh38#180117112-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49861635-C-A

180117112-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49861635-C-G

180117113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49861634-C-T

180117145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49861585-G-A

180117145-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49861585-G-T

180118655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 49861080-C-T

180118667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 49861068-C-T

180118734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49861001-G-A

180118734-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49861001-G-C

180118746-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49860989-G-C

180118920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49860816-G-A

180118935-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49860803-C-G

180118935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49860803-C-T

http://identifiers.org/hco/5/GRCh38#180119016-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49860747-C-A

180119016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49860747-C-T

180119153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49860591-C-T

180119166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49860578-G-A

180119166-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49860578-G-T

180119245-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49860525-G-C

180119245-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49860525-G-T

180119322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49860448-C-T

180119423-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 49860346-T-C

http://identifiers.org/hco/5/GRCh38#180119429-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49860340-C-A

180119429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 49860340-C-T

180119451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 49860318-G-A

180119468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49860301-G-A

180119468-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49860301-G-T

180119510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49860262-G-A

180119510-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49860262-G-T

180119570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49860202-G-A

180119570-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49860202-G-T

180120238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49860009-G-A

180120281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49859964-C-T

180120324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49859910-C-T

180120368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49859851-C-T

180120397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49859825-C-T

180120649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49858544-C-T

http://identifiers.org/hco/5/GRCh38#180120965-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49858308-C-A

180121144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 49858167-G-A

http://identifiers.org/hco/5/GRCh38#180121219-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49858105-C-A

180121219-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49858105-C-G

180121248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49858072-G-A

180121250-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49858070-T-A

180121250-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49858070-T-G

180121303-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49858018-T-G

180121803-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49857694-T-A

180122056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49857408-C-T

180127014-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49852593-A-G

180127075-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 49852532-G-A

180127178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49852448-C-T

http://identifiers.org/hco/5/GRCh38#180127195-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#49852431-A-C

180127203-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 49852423-T-G

180127230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 49852396-G-A

http://identifiers.org/hco/5/GRCh38#180127242-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49852384-A-C

180127242-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49852384-A-G

180127254-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 49852372-A-T

180127395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49852237-C-T

180127426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49852211-C-T

http://identifiers.org/hco/5/GRCh38#180127504-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49852160-C-A

180127507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49852157-G-A

180127507-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49852157-G-T

180127535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49852129-C-T

http://identifiers.org/hco/5/GRCh38#180127649-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49852013-A-C

180127687-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 49851975-C-G

180127687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 49851975-C-T

180127737-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49851918-T-C

180127737-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49851918-T-G

http://identifiers.org/hco/5/GRCh38#180127738-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49851917-C-A

180127738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49851917-C-T

http://identifiers.org/hco/5/GRCh38#180127805-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49851859-C-A

180127805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49851859-C-T

180128522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 49851311-G-A

180128579-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 49851254-T-C

180128591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 49851242-T-C

180128593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 49851240-C-T

180128917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49850840-A-G

180128917-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49850840-A-T

180129005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49850759-G-A

180135907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49849991-C-T

180135909-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49849989-T-C

180136084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49849854-A-G

180136140-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49849798-C-G

http://identifiers.org/hco/5/GRCh38#180136226-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49849716-C-A

180136226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49849716-C-T

180136241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49849701-G-A

180136241-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49849701-G-T

180136251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49849685-G-A

180136251-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49849685-G-C

180136251-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49849685-G-T

180136277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49849668-G-A

180136277-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49849668-G-T

180136281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49849664-G-A

180136281-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49849664-G-C

180136281-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49849664-G-T

180136290-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49849655-A-T

http://identifiers.org/hco/5/GRCh38#180136318-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49849630-C-A

180136318-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49849630-C-G

180136442-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 49849498-A-G

180136529-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49849410-A-G

http://identifiers.org/hco/5/GRCh38#180136579-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49849366-C-A

180136579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 49849366-C-T

http://identifiers.org/hco/5/GRCh38#180136599-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49849353-C-A

180136599-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 49849353-C-G

180136599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 49849353-C-T

180136600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 49849352-G-A

180136600-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 49849352-G-T

180136610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 49849340-G-A

180136610-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 49849340-G-T

180136611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 49849339-G-A

180136611-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 49849339-G-T

http://identifiers.org/hco/5/GRCh38#180136637-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49849278-A-C

180136637-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 49849278-A-G

180136637-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 49849278-A-T

180136643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 49849272-G-A

180136643-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 49849272-G-C

180136643-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 49849272-G-T

180136652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 49849263-G-A

180136652-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 49849263-G-C

180136652-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 49849263-G-T

180136670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 49849246-G-A

180136670-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 49849246-G-T

http://identifiers.org/hco/5/GRCh38#180136757-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49849156-C-A

180136757-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 49849156-C-G

180136757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 49849156-C-T

180136770-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 49849131-T-A

180136770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 49849131-T-C

180136770-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 49849131-T-G

180136812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49849090-G-A

180136812-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49849090-G-C

180136812-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49849090-G-T

180136830-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49849065-G-C

180136830-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49849065-G-T

180136851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49849044-G-A

180136851-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49849044-G-T

180136853-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49849042-A-G

http://identifiers.org/hco/5/GRCh38#180136882-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49849015-C-A

180136882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49849015-C-T

180136889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49849008-G-A

180136889-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49849008-G-C

180136889-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49849008-G-T

180136909-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49848988-A-G

180137011-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49848903-G-C

180137015-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49848899-C-G

180137015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49848899-C-T

180137021-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49848882-A-T

180137064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49848834-G-A

180137064-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49848834-G-C

180137074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49848823-G-A

http://identifiers.org/hco/5/GRCh38#180137190-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49848704-C-A

http://identifiers.org/hco/5/GRCh38#180137223-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49848679-A-C

180137223-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49848679-A-G

180137267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49848632-G-A

180137289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49848588-G-A

180137346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49848510-G-A

180137455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49848414-A-G

180137456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49848413-G-A

http://identifiers.org/hco/5/GRCh38#180137461-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49848408-A-C

180137473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49848398-G-A

180137473-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49848398-G-T

http://identifiers.org/hco/5/GRCh38#180137501-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49848371-C-A

180137501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49848371-C-T

180137502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49848370-A-G

http://identifiers.org/hco/5/GRCh38#180137511-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49848361-C-A

180137511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49848361-C-T

180137524-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49848348-G-T

180137525-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49848347-C-G

180137525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49848347-C-T

180137573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49848327-C-T

180137764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49848148-G-A

180137764-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49848148-G-T

180138007-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 49847910-G-T

180138060-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: 5_prime_UTR_variant, splice_acceptor_variant
orthologous variants: 49847857-T-A

180138060-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: 5_prime_UTR_variant, splice_acceptor_variant
orthologous variants: 49847857-T-C

180138060-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: 5_prime_UTR_variant, splice_acceptor_variant
orthologous variants: 49847857-T-G

http://identifiers.org/hco/5/GRCh38#180138116-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49847829-C-A

180138116-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 49847829-C-G

180138116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 49847829-C-T

180138117-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 49847828-T-A

180138117-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 49847828-T-C

180138117-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 49847828-T-G

180138150-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 49847793-T-A

180138150-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 49847793-T-C

180138150-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 49847793-T-G

180138196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 49847753-G-A

180138196-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 49847753-G-T

http://identifiers.org/hco/5/GRCh38#180138250-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49847699-C-A

180138250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 49847699-C-T

180138268-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 49847680-T-A

180138268-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 49847680-T-C

180138268-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 49847680-T-G

http://identifiers.org/hco/5/GRCh38#180138271-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49847677-C-A

180138271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 49847677-C-T

http://identifiers.org/hco/5/GRCh38#180138278-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49847670-C-A

180138278-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 49847670-C-G

180138278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 49847670-C-T

180138303-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 49847631-T-C

180138303-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 49847631-T-G

180138321-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 49847558-G-T

http://identifiers.org/hco/5/GRCh38#180138328-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49847534-C-A

180138339-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 49847523-T-C

180138339-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 49847523-T-G

180138343-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 49847519-T-C

180138343-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 49847519-T-G

http://identifiers.org/hco/5/GRCh38#180138344-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49847518-C-A

180138344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 49847518-C-T

http://identifiers.org/hco/5/GRCh38#180138354-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49847508-C-A

180138354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49847508-C-T

180138384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49847454-T-C

http://identifiers.org/hco/5/GRCh38#180138450-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49847391-A-C

http://identifiers.org/hco/5/GRCh38#180138498-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49847345-C-A

180138498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49847345-C-T

180138539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49847300-C-T

180138576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49847251-C-T

180138578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49847249-C-T

180138637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49847179-C-T

180138671-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49847154-T-C

180138998-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49846985-C-G

180139012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49846971-C-T

180139068-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49846915-A-G

180139082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49846898-G-A

180139098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49846886-C-T

180139139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49846863-G-A

180139166-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49846836-G-T

180139200-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49846805-A-G

180139454-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49846650-G-T

180139456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49846648-C-T

180139552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49846555-G-A

180139691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49846418-G-A

180139716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49846384-G-A

180139723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49846377-G-A

180139741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49846356-C-T

180154284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49842709-C-T

180154384-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49842610-G-C

http://identifiers.org/hco/5/GRCh38#180155074-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49841354-C-A

http://identifiers.org/hco/5/GRCh38#180155221-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49841208-C-A

180155221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49841208-C-T

180155445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49841036-C-T

180155600-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49840806-T-C

http://identifiers.org/hco/5/GRCh38#180155917-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49839520-C-A

180155917-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49839520-C-G

180155917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49839520-C-T

180156159-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49839203-T-C

180156183-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron_variant, undefined
orthologous variants: 49839179-T-C

180160426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49834839-G-A

180160865-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49833964-T-C

180160972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49833855-C-T

180161865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49833016-G-A

180162082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49832771-G-A

180162173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49832687-C-T

180162291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49832601-G-A

180162292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49832600-C-T

180162564-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49832383-A-G

180162601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49832347-C-T

http://identifiers.org/hco/5/GRCh38#180169359-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49830697-A-C

180169431-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49830647-C-G

180169431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49830647-C-T

180169800-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49830311-G-C

180169800-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49830311-G-T

180169872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49830192-C-T

180170307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49829666-C-T

180170336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49829635-G-A

180170381-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49829591-A-G

180170430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49829542-G-A

180170608-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49829409-T-G

180170684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49829344-C-T

180170736-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49829298-C-G

180171182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49828054-C-T

180171402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49827786-C-T

180171417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49827771-G-A

180171549-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49827653-C-G

180171549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49827653-C-T

http://identifiers.org/hco/5/GRCh38#180171586-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49827617-C-A

180172048-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49827180-T-C

http://identifiers.org/hco/5/GRCh38#180172258-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49827037-C-A

http://identifiers.org/hco/5/GRCh38#180172353-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49826921-C-A

180172407-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49826872-C-G

180172464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49826835-G-A

http://identifiers.org/hco/5/GRCh38#180172559-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49826735-C-A

180172704-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49826593-C-T

180172956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49826446-G-A

180173155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49826167-G-A

http://identifiers.org/hco/5/GRCh38#180173270-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49826057-C-A

180173280-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49826047-G-C

180173296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49826030-G-A

180173603-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49825705-T-G

180174474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49825043-G-A

180174510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49825007-G-A

180176244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49823052-C-T

180176293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49822989-G-A

180176293-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49822989-G-T

180176938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49822596-G-A

180176943-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49822591-G-T

http://identifiers.org/hco/5/GRCh38#180177059-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49822476-C-A

180177059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49822476-C-T

180177263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49822313-G-A

180177322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron_variant, undefined
orthologous variants: 49822244-C-T

180177343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron_variant, undefined
orthologous variants: 49822223-C-T

180177407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49822165-G-A

http://identifiers.org/hco/5/GRCh38#180177480-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#49822056-C-A

180177480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron_variant, undefined
orthologous variants: 49822056-C-T

180177605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron_variant, undefined
orthologous variants: 49821928-G-A

180177676-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49821857-T-C

180178832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49819683-G-A

180178838-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49819677-C-G

180178839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49819670-C-T

180178844-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49819665-G-C

180178865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49819644-G-A

180178908-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49819598-G-C

180178908-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49819598-G-T

180178974-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49819519-T-C

http://identifiers.org/hco/5/GRCh38#180179016-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49819466-C-A

180179016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49819466-C-T

180179049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49819429-C-T

180179081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49819414-G-A

180179083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49819412-G-A

180179097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49819398-G-A

180179114-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49819382-A-G

180179256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49819127-C-T

180179425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49818946-G-A

180179437-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49818929-G-T

180179508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49818833-C-T

180179607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49818747-G-A

180179609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49818745-G-A

180179610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49818744-G-A

180179610-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49818744-G-C

180179612-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49818742-T-G

180179618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49818734-G-A

180179650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49818704-G-A

http://identifiers.org/hco/5/GRCh38#180179651-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49818703-C-A

180180377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49817926-G-A

http://identifiers.org/hco/5/GRCh38#180180418-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49817886-A-C

180180470-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49817830-A-G

180180487-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49817811-C-G

180180772-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49817527-C-G

180180800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49817499-C-T

180180816-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49817482-A-G

180180924-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49817370-G-T

180181150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49817059-G-A

180181310-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49816769-A-G

http://identifiers.org/hco/5/GRCh38#180181320-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49816759-A-C

180181580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49816560-G-A

http://identifiers.org/hco/5/GRCh38#180181589-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49816551-C-A

180181589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49816551-C-T

http://identifiers.org/hco/5/GRCh38#180181628-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49816512-C-A

180181628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49816512-C-T

180194054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49809971-G-A

180194054-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49809971-G-T

180194081-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49809940-G-T

180194083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49809935-G-A

180194197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49809830-G-A

180194581-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49809433-T-G

180195079-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49808606-T-A

180195184-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49808526-G-T

180196897-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49806009-T-C

180197234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49805702-G-A

http://identifiers.org/hco/5/GRCh38#180206707-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49795214-A-C

180207193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49794791-G-A

180207400-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49794572-G-A

180207606-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49794235-G-C

180207733-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49794054-G-C

http://identifiers.org/hco/5/GRCh38#180207793-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49793996-C-A

180207793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49793996-C-T

180207859-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49793889-A-G

180207860-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49793888-C-G

180207877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49793870-C-T

180207880-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49793867-G-C

http://identifiers.org/hco/5/GRCh38#180207892-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49793855-C-A

180207897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49793851-G-A

180207941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49793811-C-T

180207986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49793785-C-T

180208038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49793733-G-A

180208524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49793343-G-A

180208545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49793324-G-A

180208545-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49793324-G-C

http://identifiers.org/hco/5/GRCh38#180208737-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#49793170-A-C

180208787-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49793119-C-G

http://identifiers.org/hco/5/GRCh38#180208919-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49792900-C-A

180208919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49792900-C-T

180208929-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49792891-C-G

180208929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: intron variant
orthologous variants: 49792891-C-T

180209126-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: 5 prime UTR variant
orthologous variants: 49792687-C-G

http://identifiers.org/hco/5/GRCh38#180209167-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#49792670-C-A

180209167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27400
most severe consequence: 5 prime UTR variant
orthologous variants: 49792670-C-T