18387356-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: 5 prime UTR variant
orthologous variants: 47347327-T-C

18387523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47347490-A-G

18387564-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47347534-A-G

18387564-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47347534-A-T

18387607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47347575-G-A

18387607-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47347575-G-T

18387609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47347577-A-G

18387609-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47347577-A-T

18387651-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47347617-A-G

18387651-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47347617-A-T

18387665-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47347636-T-G

18387840-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47347823-G-C

18387840-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47347823-G-T

http://identifiers.org/hco/6/GRCh38#18387920-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#47347898-A-C

18388077-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47348119-A-G

18388269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47348253-C-T

18388274-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47348258-G-C

18388360-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47348329-A-G

18388382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47348350-G-A

18388686-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47348654-C-G

18388924-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47348956-T-C

18389025-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47349062-A-T

18389287-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47349345-T-G

18389588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47349691-T-C

18389598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47349701-C-T

18389753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47349855-A-G

18389933-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47350029-A-T

18390016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47350089-G-A

18390072-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47350144-C-G

18390356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47350700-G-A

18390356-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47350700-G-T

18390935-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47351498-G-C

18391209-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47351779-A-T

18391222-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47351792-A-G

18391377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47351949-G-A

18391401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47351970-A-G

18392419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47352353-C-T

18392659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47353293-C-T

http://identifiers.org/hco/6/GRCh38#18392860-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#47353485-C-A

18393151-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47353531-T-C

18393186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47353566-C-T

18393388-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47353775-G-C

18393524-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47353904-T-C

18393539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47353919-G-A

18393590-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47353971-C-G

http://identifiers.org/hco/6/GRCh38#18393737-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#47354785-C-A

18393737-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47354785-C-G

18393737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47354785-C-T

18393784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47354830-T-C

18394634-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47355516-A-G

18394649-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47355532-A-G

18394924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47355812-C-T

18394929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47355817-C-T

18394930-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47355818-A-G

18395273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47356176-G-A

18395318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47356218-A-G

18395399-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47356690-G-T

18395459-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47356746-A-G

http://identifiers.org/hco/6/GRCh38#18395858-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#47357188-A-C

18395985-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47357294-A-G

http://identifiers.org/hco/6/GRCh38#18396229-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#47357536-C-A

http://identifiers.org/hco/6/GRCh38#18399040-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#47360362-C-A

18399121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47360449-C-T

18399127-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47360455-T-C

18399175-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47360507-C-G

18399320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47360655-C-T

18399382-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47360712-G-C

18399382-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47360712-G-T

18399439-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47360770-T-G

18399547-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 47360874-G-T

18399616-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 47360943-A-G

18399634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 47360961-C-T

18399699-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 47361026-T-C

18400268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47361365-G-A

18400268-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47361365-G-T

18400625-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47361676-G-C

18400636-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47361687-T-C

http://identifiers.org/hco/6/GRCh38#18400684-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#47361735-A-C

18400757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47361809-C-T

18400837-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47362020-C-G

18400871-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47362194-C-G

18401007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47362326-C-T

http://identifiers.org/hco/6/GRCh38#18401021-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#47362337-A-C

18401065-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47362386-T-C

18401067-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47362388-G-T

18401150-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47362502-A-G

18401151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47362503-A-G

18401352-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47362707-C-G

18401352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47362707-C-T

http://identifiers.org/hco/6/GRCh38#18402666-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#47363338-A-C

18402815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47363467-G-A

18402866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47363521-A-G

18402992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47363612-G-A

18403004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47363624-C-T

18403045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47363664-G-A

http://identifiers.org/hco/6/GRCh38#18403478-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#47364766-C-A

18403478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47364766-C-T

18404912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47366180-C-T

18405021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47366274-C-T

18405038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47366297-G-A

http://identifiers.org/hco/6/GRCh38#18405653-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#47366569-C-A

18405654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47366570-C-T

18405689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47366600-G-A

18405702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47366614-G-A

18405763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47366675-G-A

18405911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47366823-C-T

18405993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47366902-G-A

18406047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47366952-G-A

18406172-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47367075-C-G

18406189-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47367089-A-G

18415647-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47369480-A-G

18415743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47369574-T-C

18415836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47369648-G-A

18423452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47370532-C-T

18423454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47370534-C-T

18423521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47370581-C-T

18423707-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47370755-A-T

18423841-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47370893-T-C

18424129-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47371139-A-G

http://identifiers.org/hco/6/GRCh38#18424179-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#47371192-C-A

18424209-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47371222-C-G

18424648-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47371603-C-G

http://identifiers.org/hco/6/GRCh38#18424772-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#47371714-C-A

18424781-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47371723-T-G

18425184-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47371900-T-A

18425184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47371900-T-C

18425336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47372051-A-G

18425349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47372064-G-A

http://identifiers.org/hco/6/GRCh38#18425500-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#47372167-A-C

18425668-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47372332-G-C

18425781-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47372446-T-C

18425949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47372605-G-A

18425949-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47372605-G-C

18426080-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47372735-G-T

http://identifiers.org/hco/6/GRCh38#18426205-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#47372840-C-A

18426342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47372983-C-T

18427332-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47373713-A-T

http://identifiers.org/hco/6/GRCh38#18427450-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#47373832-A-C

18427450-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47373832-A-T

18427504-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47373883-A-T

18427682-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 47374071-T-C

18428493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47374559-C-T

18428577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47374629-G-A

18428604-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47374651-A-T

18428756-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47374812-A-G

18428827-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47374882-A-G

18428856-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47374905-T-G

18428907-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47374953-G-T

18429270-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47374993-G-C

18429893-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47375828-T-C

18429895-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47375830-T-G

18429988-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47375930-A-T

18429991-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47375933-A-G

18430143-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47376057-A-G

18430143-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47376057-A-T

18430235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47376156-C-T

18430266-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47376186-A-T

18430460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47376334-A-G

18430811-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47376496-T-G

18430812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47376497-C-T

18430892-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47376583-T-C

18431132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47376746-G-A

18431218-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47376785-T-C

18431480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47376999-G-A

18431841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47377255-C-T

18432973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47378087-A-G

18433044-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47378159-A-G

18433079-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47378195-G-C

18433802-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47378753-A-G

18434051-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47379011-A-G

18434051-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47379011-A-T

18434174-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47379120-A-G

18434195-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47379140-C-G

18434195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47379140-C-T

18434412-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47379372-T-A

18434451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47379413-C-T

18436071-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47380337-A-G

http://identifiers.org/hco/6/GRCh38#18436081-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#47380347-A-C

18436081-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47380347-A-T

18436218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47380486-A-G

18436275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47380543-T-C

18436384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47380645-T-C

18438355-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47381004-A-T

18438396-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47381040-T-C

18438561-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47381214-T-C

18439142-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47381946-A-G

18439242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47382025-C-T

http://identifiers.org/hco/6/GRCh38#18439264-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#47382047-C-A

18439386-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47382164-T-A

18439577-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47382309-G-T

18439610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47382341-A-G

18439633-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47382366-T-G

18439674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47382407-C-T

18439767-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47382499-T-C

18439769-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47382501-A-T

18439773-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47382505-T-C

18439792-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47382525-G-T

18439973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47382727-A-G

18440033-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47382791-A-G

18440075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47382836-A-G

18440095-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47382857-C-G

18440096-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47382858-A-G

18440118-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47382882-A-G

18440151-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47382920-C-G

18440226-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47382997-A-G

18440410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47383193-G-A

18440447-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47383216-G-T

18440590-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47383356-T-C

18440696-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47383464-A-G

18440751-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47383517-G-C

18440841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47383564-C-T

18441919-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47383938-G-A

18442103-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47384134-A-T

18442471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47384663-C-T

18445245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47385599-A-G

18445274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47385628-G-A

18445274-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47385628-G-C

18445463-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47385888-A-G

18445537-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47385947-G-C

18449008-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47387385-A-G

http://identifiers.org/hco/6/GRCh38#18449077-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#47387457-A-C

18449268-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47387618-A-G

18449311-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47387664-C-G

18449379-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47387730-A-G

18450043-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47387934-A-G

18453862-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47388997-A-G

18453869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47389004-C-T

18453951-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47389083-A-G

http://identifiers.org/hco/6/GRCh38#18454304-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#47389366-C-A

18454362-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47389422-G-C

18454367-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47389427-A-G

18454641-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47389793-C-G

18454857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47389974-C-T

http://identifiers.org/hco/6/GRCh38#18455806-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#47390222-C-A

18455848-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47390267-G-T

18456261-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47390319-T-C

18456425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47390431-G-A

18456616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47390616-G-A

18457090-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47390812-T-C

18457114-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47390836-G-T

18457225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: synonymous variant
orthologous variants: 47390949-G-A

18457225-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: synonymous variant
orthologous variants: 47390949-G-T

http://identifiers.org/hco/6/GRCh38#18457366-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#47391084-A-C

18457437-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron_variant, undefined
orthologous variants: 47391152-T-A

http://identifiers.org/hco/6/GRCh38#18457472-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#47391173-C-A

18457472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47391173-C-T

18457594-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47391290-G-C

18458305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47391777-T-C

18458540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47391995-C-T

18458568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47392017-G-A

18458959-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47392548-G-T

18459070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47392659-G-A

18459246-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47392846-A-T

18459465-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47393059-A-G

18459465-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47393059-A-T

http://identifiers.org/hco/6/GRCh38#18459517-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#47393106-C-A

18459517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47393106-C-T

18459631-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: synonymous variant
orthologous variants: 47393217-A-G

http://identifiers.org/hco/6/GRCh38#18459815-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#47393403-C-A

18459815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47393403-C-T

18460029-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47393773-T-C

18460070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47393811-C-T

18460100-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47393841-A-G

http://identifiers.org/hco/6/GRCh38#18460280-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#47394003-A-C

18460394-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47394115-T-A

18460505-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47394193-A-T

18460651-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47394238-C-G

18460678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47394265-C-T

18461857-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47395299-T-C

18462070-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47395469-A-G

18462070-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47395469-A-T

18462072-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47395471-G-A

http://identifiers.org/hco/6/GRCh38#18462493-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#47395808-A-C

18462632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47395888-C-T

http://identifiers.org/hco/6/GRCh38#18462660-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#47395905-A-C

18462660-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47395905-A-T

18462688-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47395911-T-C

18462700-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47395923-G-T

18462879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47396060-C-T

18462882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47396063-T-C

18463277-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47396326-T-C

18463341-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: synonymous variant
orthologous variants: 47396390-T-C

http://identifiers.org/hco/6/GRCh38#18463414-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#47396463-C-A

http://identifiers.org/hco/6/GRCh38#18463418-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#47396467-A-C

18463418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47396467-A-G

18463601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47396595-C-T

18463707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47396698-C-T

18464236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47396858-G-A

18464485-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47397128-T-C

18464647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47397592-G-A

18464647-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47397592-G-C

http://identifiers.org/hco/6/GRCh38#18464759-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#47397671-C-A

18464759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47397671-C-T

18464786-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47397698-A-G

18464786-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: intron variant
orthologous variants: 47397698-A-T

18464932-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: synonymous variant
orthologous variants: 47397842-G-T

18464935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: synonymous variant
orthologous variants: 47397845-G-A

18465089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: 3 prime UTR variant
orthologous variants: 47397988-C-T

18465098-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: 3 prime UTR variant
orthologous variants: 47397997-T-G

http://identifiers.org/hco/6/GRCh38#18465212-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#47398111-C-A

18465326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: 3 prime UTR variant
orthologous variants: 47398240-T-C

http://identifiers.org/hco/6/GRCh38#18465339-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#47398253-C-A

18465340-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: 3 prime UTR variant
orthologous variants: 47398254-A-G

18465397-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: 3 prime UTR variant
orthologous variants: 47398310-T-C

18465505-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: 3 prime UTR variant
orthologous variants: 47398413-A-G

18465507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: 3 prime UTR variant
orthologous variants: 47398415-G-A

18465507-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: 3 prime UTR variant
orthologous variants: 47398415-G-T

18465536-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: 3 prime UTR variant
orthologous variants: 47398444-A-G

18465536-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: 3 prime UTR variant
orthologous variants: 47398444-A-T

18465602-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: 3 prime UTR variant
orthologous variants: 47398509-T-A

18465669-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: 3 prime UTR variant
orthologous variants: 47398577-G-T

18465959-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: 3 prime UTR variant
orthologous variants: 47398868-T-G

http://identifiers.org/hco/6/GRCh38#18466166-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#47399072-A-C

18466394-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: 3 prime UTR variant
orthologous variants: 47399302-G-C

18466684-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: 3 prime UTR variant
orthologous variants: 47399566-G-C

18466786-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: 3 prime UTR variant
orthologous variants: 47399729-A-G

18466864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: 3 prime UTR variant
orthologous variants: 47399852-T-C

18466958-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: 3 prime UTR variant
orthologous variants: 47399939-T-G

18467218-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: 3 prime UTR variant
orthologous variants: 47400204-T-A

18467218-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: 3 prime UTR variant
orthologous variants: 47400204-T-G

http://identifiers.org/hco/6/GRCh38#18467281-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#47400257-A-C

http://identifiers.org/hco/6/GRCh38#18467422-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#47400400-C-A

18467422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: 3 prime UTR variant
orthologous variants: 47400400-C-T

18467425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: 3 prime UTR variant
orthologous variants: 47400403-G-A

18467425-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: 3 prime UTR variant
orthologous variants: 47400403-G-T

http://identifiers.org/hco/6/GRCh38#18467429-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#47400407-A-C

18467429-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: 3 prime UTR variant
orthologous variants: 47400407-A-G

18467429-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: 3 prime UTR variant
orthologous variants: 47400407-A-T

18467433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: 3 prime UTR variant
orthologous variants: 47400411-A-G

18467433-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: 3 prime UTR variant
orthologous variants: 47400411-A-T

18467443-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: 3 prime UTR variant
orthologous variants: 47400421-G-T

http://identifiers.org/hco/6/GRCh38#18467638-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#47400634-C-A

18467638-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: 3 prime UTR variant
orthologous variants: 47400634-C-G

18468272-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: 3 prime UTR variant
orthologous variants: 47400859-A-G

18468366-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 47400958-A-G

http://identifiers.org/hco/6/GRCh38#18468467-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#47401060-A-C

http://identifiers.org/hco/6/GRCh38#18468524-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21578
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#47401126-C-A