28300572-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: 3 prime UTR variant
orthologous variants: 147498623-T-A

28300572-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: 3 prime UTR variant
orthologous variants: 147498623-T-C

28300595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: 3 prime UTR variant
orthologous variants: 147498650-C-T

28300671-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: 3 prime UTR variant
orthologous variants: 147498690-G-T

28300971-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: 3 prime UTR variant
orthologous variants: 147499001-C-G

http://identifiers.org/hco/13/GRCh38#28301164-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147499198-C-A

http://identifiers.org/hco/13/GRCh38#28301329-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147499326-C-A

28301445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: 3 prime UTR variant
orthologous variants: 147499439-G-A

28301445-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: 3 prime UTR variant
orthologous variants: 147499439-G-T

28301644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: 3 prime UTR variant
orthologous variants: 147499603-C-T

http://identifiers.org/hco/13/GRCh38#28301648-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147499607-C-A

28301648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: 3 prime UTR variant
orthologous variants: 147499607-C-T

28301857-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: 3 prime UTR variant
orthologous variants: 147499831-G-C

28301857-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: 3 prime UTR variant
orthologous variants: 147499831-G-T

28302069-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: 3 prime UTR variant
orthologous variants: 147500021-G-T

http://identifiers.org/hco/13/GRCh38#28302291-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147500242-C-A

http://identifiers.org/hco/13/GRCh38#28302306-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147500260-C-A

28302394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: 3 prime UTR variant
orthologous variants: 147500388-C-T

28302557-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: 3 prime UTR variant
orthologous variants: 147500534-G-T

28302559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: 3 prime UTR variant
orthologous variants: 147500536-G-A

28302559-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: 3 prime UTR variant
orthologous variants: 147500536-G-T

28302592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: 3 prime UTR variant
orthologous variants: 147500569-T-C

28302622-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: 3 prime UTR variant
orthologous variants: 147500603-T-C

28302745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: 3 prime UTR variant
orthologous variants: 147500676-G-A

28302794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: 3 prime UTR variant
orthologous variants: 147500726-G-A

28302794-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: 3 prime UTR variant
orthologous variants: 147500726-G-C

28302794-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: 3 prime UTR variant
orthologous variants: 147500726-G-T

28302829-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: 3 prime UTR variant
orthologous variants: 147500751-T-G

28302830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: 3 prime UTR variant
orthologous variants: 147500755-G-A

28302830-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: 3 prime UTR variant
orthologous variants: 147500755-G-T

28302846-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: 3 prime UTR variant
orthologous variants: 147500771-T-C

28302883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: 3 prime UTR variant
orthologous variants: 147500819-G-A

28302883-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: 3 prime UTR variant
orthologous variants: 147500819-G-T

28302960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: 3 prime UTR variant
orthologous variants: 147500843-G-A

28302960-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: 3 prime UTR variant
orthologous variants: 147500843-G-C

28302960-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: 3 prime UTR variant
orthologous variants: 147500843-G-T

28302962-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: 3 prime UTR variant
orthologous variants: 147500845-T-A

28302964-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: 3 prime UTR variant
orthologous variants: 147500847-T-C

28303066-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 147500963-G-T

28303197-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 147501060-C-G

28303197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 147501060-C-T

http://identifiers.org/hco/13/GRCh38#28303503-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147501330-C-A

28303503-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147501330-C-G

28303503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147501330-C-T

28303950-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147501910-G-T

http://identifiers.org/hco/13/GRCh38#28304112-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147502082-C-A

28304112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147502082-C-T

28304246-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147502251-A-G

28304292-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147502301-T-C

28306198-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147502778-C-G

28306206-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147502786-A-G

28306296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147502865-G-A

28306334-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147502890-C-G

28306337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147502893-C-T

28306559-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147503116-G-T

28306578-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147503128-G-T

28306631-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147503180-T-A

28306631-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147503180-T-C

28306700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 147503232-G-A

28306783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147503315-A-G

28306789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147503322-A-G

28306797-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147503330-T-C

28307336-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147504300-T-C

28307399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147504353-C-T

28307400-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147504354-G-A

28307469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147504418-T-C

28307478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147504425-C-T

28307572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147504521-C-T

28308334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147504873-G-A

28308334-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147504873-G-C

28308396-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 147504935-A-G

28308396-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 147504935-A-T

http://identifiers.org/hco/13/GRCh38#28308403-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147504942-C-A

28308403-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 147504942-C-G

28308403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 147504942-C-T

28308428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 147504966-G-A

28308512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147505039-C-T

28308589-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147505269-T-A

28308589-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147505269-T-C

28308712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147505435-G-A

28308712-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147505435-G-T

http://identifiers.org/hco/13/GRCh38#28308723-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147505446-C-A

28308723-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147505446-C-G

http://identifiers.org/hco/13/GRCh38#28308735-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147505458-C-A

28308735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147505458-C-T

28308758-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147505481-A-T

28308830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147505539-C-T

28308939-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147505648-A-G

28308985-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147505699-T-A

28308985-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147505699-T-C

http://identifiers.org/hco/13/GRCh38#28309034-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147505740-A-C

28309034-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147505740-A-G

28309074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147505786-G-A

28309083-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147505795-G-T

28309390-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147506262-G-T

28309423-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147506291-G-C

28309423-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147506291-G-T

28309498-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147506358-A-G

http://identifiers.org/hco/13/GRCh38#28309575-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147506434-C-A

28309770-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147506557-G-C

28311285-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147507408-A-G

28311321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147507442-C-T

28311386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147507517-G-A

28311386-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147507517-G-C

28311414-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147507548-G-C

28311440-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147507574-G-T

28311604-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 147507688-G-A

28311625-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 147507709-A-G

28311995-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 147508263-G-T

http://identifiers.org/hco/13/GRCh38#28312002-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147508270-A-C

28312125-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147508392-A-G

28312172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147508436-G-A

28312172-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147508436-G-T

http://identifiers.org/hco/13/GRCh38#28312179-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147508443-C-A

28312179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147508443-C-T

28312198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147508463-G-A

28312198-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147508463-G-C

28312198-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147508463-G-T

http://identifiers.org/hco/13/GRCh38#28312222-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147508484-C-A

28312222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147508484-C-T

28312629-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147508780-C-T

28312817-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 147509048-G-C

28312853-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147509080-G-T

28312854-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 147509081-C-G

28312854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 147509081-C-T

28314433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147509890-C-T

28314439-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147509900-G-C

28314486-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147509946-A-G

28315084-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147510787-G-T

28315160-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147510857-T-C

28315732-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147511006-T-G

http://identifiers.org/hco/13/GRCh38#28315776-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147511046-A-C

28315776-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147511046-A-G

28316013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147511221-G-A

28316258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147511449-G-A

28316383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147511577-C-T

28316422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147511616-C-T

28316845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147512199-A-G

28316854-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147512223-C-G

28316866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147512240-G-A

28316949-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147512412-A-G

28317012-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147512492-C-G

28317033-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147512505-A-G

28317054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147512527-G-A

28317111-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147512578-T-C

http://identifiers.org/hco/13/GRCh38#28317246-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147512689-C-A

28317345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147512789-C-T

http://identifiers.org/hco/13/GRCh38#28317386-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147512840-C-A

28317386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147512840-C-T

http://identifiers.org/hco/13/GRCh38#28317416-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147512876-A-C

28317416-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147512876-A-G

28317440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147512892-G-A

28317440-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147512892-G-T

28317475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147512920-A-G

28317475-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147512920-A-T

http://identifiers.org/hco/13/GRCh38#28317641-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147513092-A-C

28317641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147513092-A-G

28317661-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147513112-G-T

28317671-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147513253-A-G

28317878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147513567-G-A

28317893-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147513580-T-A

28318004-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147513635-G-C

28318174-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147513692-A-T

28318280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147513777-C-T

28318286-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147513784-A-T

28318595-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 147514053-T-G

28318646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 147514104-G-A

28318698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 147514156-G-A

28318723-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 147514181-A-G

28319022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147514828-G-A

http://identifiers.org/hco/13/GRCh38#28319023-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147514829-C-A

28319023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147514829-C-T

28319058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147514861-C-T

28319059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147514862-G-A

28319116-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147514912-A-G

28319139-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147514939-A-G

http://identifiers.org/hco/13/GRCh38#28319293-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147515016-C-A

28319293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147515016-C-T

28319341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147515051-G-A

28319341-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147515051-G-C

28319341-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147515051-G-T

28319354-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147515066-A-T

28319376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147515088-G-A

28319376-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147515088-G-C

28319376-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147515088-G-T

28319444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 147515156-G-A

28319444-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 147515156-G-T

28319447-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 147515159-A-G

28319469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 147515181-G-A

28319538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 147515250-G-A

28319552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147515264-G-A

28319552-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147515264-G-T

28319603-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147515308-T-A

28319603-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147515308-T-G

http://identifiers.org/hco/13/GRCh38#28319609-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147515314-C-A

28319726-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147515400-T-C

28319903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147515567-G-A

28320115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147515826-G-A

28320208-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147515932-C-G

28320226-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147515937-A-G

28320238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147515949-G-A

28320254-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147515965-A-G

28320378-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147516093-G-T

28320459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147516158-G-A

28320681-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147516327-A-G

28321189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147516862-C-T

28321218-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147516888-C-G

28321218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147516888-C-T

28321336-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147516980-T-C

28321338-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147516982-T-C

28321338-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147516982-T-G

http://identifiers.org/hco/13/GRCh38#28321344-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147516988-C-A

28321344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147516988-C-T

28321371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147517013-G-A

28321371-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147517013-G-T

28321389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 147517030-G-A

28321389-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 147517030-G-T

28321410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147517058-G-A

28321410-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147517058-G-T

28321443-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147517091-T-C

28321456-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 147517105-G-T

http://identifiers.org/hco/13/GRCh38#28321645-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147517335-C-A

28321645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147517335-C-T

28321648-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147517338-C-G

28321648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147517338-C-T

28321649-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147517339-T-C

28321649-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147517339-T-G

28321710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147517596-G-A

28321710-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147517596-G-T

28321720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147517606-G-A

28321720-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147517606-G-C

28321720-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147517606-G-T

http://identifiers.org/hco/13/GRCh38#28321733-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147517619-C-A

28321733-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147517619-C-G

28321733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147517619-C-T

28322130-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147518170-A-T

http://identifiers.org/hco/13/GRCh38#28322157-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147518197-C-A

28322157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147518197-C-T

28322244-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147518287-G-A

28322244-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147518287-G-T

28322274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 147518925-C-T

28322304-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 147518955-A-T

28322364-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 147519015-A-G

28322465-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 147519105-G-T

http://identifiers.org/hco/13/GRCh38#28322673-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147519245-C-A

28322691-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147519258-G-T

28322740-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147519312-A-G

28322753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147519325-A-G

28322770-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147519341-A-G

28322833-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 147519404-G-T

28322835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 147519406-C-T

28322836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 147519407-G-A

28322872-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 147519440-T-A

28322912-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 147519480-T-C

28322985-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147519550-T-G

28322987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147519552-C-T

http://identifiers.org/hco/13/GRCh38#28323077-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147519604-C-A

28323077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147519604-C-T

28323795-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147520369-A-G

28323909-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147520468-A-T

28323966-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147520520-C-G

http://identifiers.org/hco/13/GRCh38#28324210-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147520785-C-A

28324279-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147520882-T-C

28324701-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147521306-G-A

28324701-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147521306-G-T

28324801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147521336-G-A

28324863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147521383-C-T

28325370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147521831-A-G

28325683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147522221-G-A

28326015-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147522837-G-C

28326080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147522939-C-T

28326100-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147522959-T-G

28326176-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147523125-T-C

28326249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147523192-C-T

28326422-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147523355-C-G

http://identifiers.org/hco/13/GRCh38#28327575-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147525445-A-C

28327575-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147525445-A-G

28327575-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147525445-A-T

http://identifiers.org/hco/13/GRCh38#28327609-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147525479-C-A

http://identifiers.org/hco/13/GRCh38#28327664-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147525534-C-A

28327664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147525534-C-T

28327665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147525535-G-A

28327665-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147525535-G-C

28327665-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147525535-G-T

28328702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147525851-G-A

http://identifiers.org/hco/13/GRCh38#28328845-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147525955-C-A

28328845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147525955-C-T

http://identifiers.org/hco/13/GRCh38#28328887-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147525985-A-C

28329168-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147526260-T-A

28329168-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147526260-T-C

28329400-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147526453-G-A

28329525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147526481-C-T

http://identifiers.org/hco/13/GRCh38#28329590-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147526547-A-C

28329590-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147526547-A-G

28329591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147526548-G-A

28329591-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147526548-G-T

28329771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147526728-G-A

28329771-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147526728-G-T

http://identifiers.org/hco/13/GRCh38#28329792-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147526761-C-A

28329792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147526761-C-T

28329932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147526893-C-T

28330122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147527077-C-T

28330178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147527138-T-C

28330279-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147527431-T-C

28330413-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147527573-T-C

28331147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147528719-G-A

28331169-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147528741-G-C

28331229-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147528801-A-G

28331238-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147528810-T-A

28331303-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147528871-A-T

28332859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147529678-G-A

28333320-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147530650-A-G

28333361-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147530690-T-G

28333694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147531034-A-G

28333864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147531225-C-T

28333931-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147531271-G-C

28333931-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147531271-G-T

28333942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147531280-C-T

28333944-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147531282-G-T

28333984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147531320-T-C

28334007-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147531342-A-G

http://identifiers.org/hco/13/GRCh38#28334017-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147531358-A-C

28334017-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 147531358-A-T

28334152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147531492-G-A

28334152-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147531492-G-T

http://identifiers.org/hco/13/GRCh38#28334252-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147531603-C-A

28334268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147531621-G-A

28334268-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147531621-G-T

http://identifiers.org/hco/13/GRCh38#28334442-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147531798-C-A

28334538-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147531860-G-C

28334599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147531913-C-T

28334625-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147531939-A-G

28334631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147531945-C-T

28334811-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147532125-G-T

28335114-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147532382-A-G

28335114-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147532382-A-T

28335191-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147532458-T-C

28335214-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147532481-T-C

28335503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147532785-C-T

28335844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147533049-C-T

28335876-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147533081-T-A

28335876-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147533081-T-C

28336027-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147533206-C-T

28336048-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147533222-T-C

28336213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147533368-C-T

28336326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147533439-T-C

http://identifiers.org/hco/13/GRCh38#28336511-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147533621-C-A

28336538-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 147533628-G-T

28337198-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147534369-A-T

28337496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147534738-G-A

28337496-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147534738-G-C

28337673-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147534897-C-G

28337673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147534897-C-T

28337714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147534940-G-A

28337749-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147534973-T-C

28338082-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147535343-T-C

28338281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147535525-C-T

28338640-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147535886-T-A

28338648-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147535903-G-T

28338652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147535907-A-G

28338662-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147535926-A-T

28338718-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147535966-T-C

28338754-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147536000-A-G

28339014-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147536208-T-C

http://identifiers.org/hco/13/GRCh38#28339030-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147536224-C-A

28339034-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147536228-T-C

28339050-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147536234-G-T

28339064-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147536248-T-G

http://identifiers.org/hco/13/GRCh38#28339089-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147536272-C-A

28339089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147536272-C-T

28339217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 147536398-G-A

28339288-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 147536469-T-C

28339315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147536508-G-A

28339315-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147536508-G-T

28340427-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147538227-A-T

28340595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147538383-G-A

28340679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 147538456-C-T

http://identifiers.org/hco/13/GRCh38#28340762-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147538539-C-A

28341060-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147538726-T-C

28341317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147538937-G-A

28341471-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147539054-A-G

28341655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147539211-C-T

28341657-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147539213-A-G

28341701-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147539257-T-C

28342459-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147539555-T-A

28342459-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147539555-T-C

28342606-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147539684-A-G

http://identifiers.org/hco/13/GRCh38#28345645-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147540506-A-C

http://identifiers.org/hco/13/GRCh38#28345707-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147540529-C-A

28345723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147540545-G-A

28345723-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147540545-G-T

28345789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 147540565-G-A

28345789-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 147540565-G-C

28345789-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 147540565-G-T

http://identifiers.org/hco/13/GRCh38#28345832-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147540603-C-A

28345893-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147540664-A-T

http://identifiers.org/hco/13/GRCh38#28345930-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147540698-A-C

28345930-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147540698-A-G

28345930-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147540698-A-T

28345935-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147540703-T-A

28345935-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147540703-T-C

28345935-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147540703-T-G

http://identifiers.org/hco/13/GRCh38#28345936-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147540704-C-A

http://identifiers.org/hco/13/GRCh38#28345980-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147540749-C-A

http://identifiers.org/hco/13/GRCh38#28346004-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147540763-C-A

28346094-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147540858-T-C

28346121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 147540884-T-C

28349362-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron variant
orthologous variants: 147543492-C-G

28349477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron variant
orthologous variants: 147543576-C-T

28349822-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron variant
orthologous variants: 147543874-C-G

28350168-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron variant
orthologous variants: 147544215-C-G

28350425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron variant
orthologous variants: 147544403-G-A

28350609-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron variant
orthologous variants: 147544670-G-C

28350640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron variant
orthologous variants: 147544700-C-T

28351144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron variant
orthologous variants: 147546405-G-A

28351338-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron variant
orthologous variants: 147546547-G-T

28351381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron variant
orthologous variants: 147546579-G-A

28351381-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron variant
orthologous variants: 147546579-G-T

28351407-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron variant
orthologous variants: 147546590-T-C

28351440-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron variant
orthologous variants: 147546607-G-C

28351560-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron variant
orthologous variants: 147546701-T-C

28351662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron variant
orthologous variants: 147546778-G-A

28351778-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron variant
orthologous variants: 147546912-T-C

28351796-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron variant
orthologous variants: 147546930-A-G

28351796-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron variant
orthologous variants: 147546930-A-T

28351844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron variant
orthologous variants: 147546977-G-A

28351990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron variant
orthologous variants: 147547108-C-T

28352276-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron variant
orthologous variants: 147547354-T-C

28352364-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron variant
orthologous variants: 147547495-T-G

28352477-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron variant
orthologous variants: 147547738-A-G

28352564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron variant
orthologous variants: 147547823-C-T

28353069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron variant
orthologous variants: 147548594-C-T

28353082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron variant
orthologous variants: 147548611-G-A

28353641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron variant
orthologous variants: 147548834-G-A

28353845-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron variant
orthologous variants: 147549024-T-C

28354014-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron variant
orthologous variants: 147549189-A-G

28354034-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron variant
orthologous variants: 147549209-C-G

28354034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron variant
orthologous variants: 147549209-C-T

28354154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron variant
orthologous variants: 147549305-G-A

28356033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron variant
orthologous variants: 147550613-C-T

28356180-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron variant
orthologous variants: 147550769-C-G

28356714-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron variant
orthologous variants: 147551113-T-A

28356724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron variant
orthologous variants: 147551123-G-A

28356724-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron variant
orthologous variants: 147551123-G-C

28357156-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron variant
orthologous variants: 147551541-A-G

28357423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron variant
orthologous variants: 147551811-A-G

28357669-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: synonymous variant
orthologous variants: 147552054-T-C

http://identifiers.org/hco/13/GRCh38#28357726-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147552111-C-A

28357760-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron variant
orthologous variants: 147552142-T-G

28357892-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron variant
orthologous variants: 147552216-G-C

28357892-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron variant
orthologous variants: 147552216-G-T

http://identifiers.org/hco/13/GRCh38#28358570-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147552657-C-A

28358570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron variant
orthologous variants: 147552657-C-T

28365908-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron variant
orthologous variants: 147559985-A-G

28366097-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron variant
orthologous variants: 147560049-G-C

28366203-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron variant
orthologous variants: 147560158-G-T

28366283-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron variant
orthologous variants: 147560240-C-G

28366298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron variant
orthologous variants: 147560254-C-T

28366477-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron variant
orthologous variants: 147560391-T-A

28366873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron variant
orthologous variants: 147560563-C-T

28367163-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron variant
orthologous variants: 147560847-T-C

28367166-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron variant
orthologous variants: 147560850-A-T

http://identifiers.org/hco/13/GRCh38#28367177-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147560862-A-C

28367177-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron variant
orthologous variants: 147560862-A-G

28367329-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron variant
orthologous variants: 147561006-T-C

28367404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron variant
orthologous variants: 147561071-G-A

28367470-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron variant
orthologous variants: 147561137-A-G

28367694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron variant
orthologous variants: 147561338-G-A

28370767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron variant
orthologous variants: 147561684-C-T

28370871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron variant
orthologous variants: 147561776-C-T

http://identifiers.org/hco/13/GRCh38#28371145-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147562017-C-A

28373520-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron variant
orthologous variants: 147563008-G-T

28373692-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron variant
orthologous variants: 147563157-T-C

28375977-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron variant
orthologous variants: 147563485-A-G

28376341-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron variant
orthologous variants: 147563780-C-G

28376416-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron variant
orthologous variants: 147563840-A-T

28376420-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron variant
orthologous variants: 147563844-T-A

28376643-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron variant
orthologous variants: 147564054-T-A

28376747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron variant
orthologous variants: 147564151-G-A

28376835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron variant
orthologous variants: 147564223-C-T

28376845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron variant
orthologous variants: 147564233-G-A

28376906-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron variant
orthologous variants: 147564276-G-T

28377104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron variant
orthologous variants: 147564496-C-T

28377276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron variant
orthologous variants: 147564632-C-T

28377700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron variant
orthologous variants: 147566228-C-T

28377711-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron variant
orthologous variants: 147566239-T-C

28377930-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron variant
orthologous variants: 147566464-T-G

28379708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron variant
orthologous variants: 147567383-C-T

28379898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron variant
orthologous variants: 147567557-G-A

28380152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron variant
orthologous variants: 147567788-G-A

28380336-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron variant
orthologous variants: 147567955-T-C

28380942-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron variant
orthologous variants: 147568364-A-G

28380942-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron variant
orthologous variants: 147568364-A-T

28381113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron variant
orthologous variants: 147568492-A-G

28381644-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron variant
orthologous variants: 147568902-A-T

http://identifiers.org/hco/13/GRCh38#28381732-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147568987-A-C

28382013-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron variant
orthologous variants: 147569218-T-C

28382014-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron variant
orthologous variants: 147569219-C-G

28382015-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron variant
orthologous variants: 147569220-T-C

28382911-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron variant
orthologous variants: 147569811-G-T

28384123-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron variant
orthologous variants: 147570467-G-C

28384496-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron variant
orthologous variants: 147570496-T-A

28384496-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron variant
orthologous variants: 147570496-T-C

28384809-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron variant
orthologous variants: 147571101-G-C

28384809-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron variant
orthologous variants: 147571101-G-T

28384850-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron variant
orthologous variants: 147571144-A-T

28384862-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron variant
orthologous variants: 147571156-T-A

28384862-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron variant
orthologous variants: 147571156-T-C

28384942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: missense variant
orthologous variants: 147571244-C-T

28384955-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: synonymous variant
orthologous variants: 147571257-A-G

28385173-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: intron variant
orthologous variants: 147571449-T-A

http://identifiers.org/hco/13/GRCh38#28385557-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147571876-C-A

http://identifiers.org/hco/13/GRCh38#28385614-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147571937-C-A

28385614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 147571937-C-T

http://identifiers.org/hco/13/GRCh38#28385660-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147571983-A-C

28385774-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 147572099-A-G

http://identifiers.org/hco/13/GRCh38#28385815-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147572141-C-A

http://identifiers.org/hco/13/GRCh38#28385837-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147572163-C-A

28385837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 147572163-C-T

28385849-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 147572175-A-G

28385849-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 147572175-A-T

28385970-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 147572280-A-G

28386006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 147572322-C-T

http://identifiers.org/hco/13/GRCh38#28386069-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147572386-C-A

28386069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 147572386-C-T

28386225-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 147572519-C-G

28386225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 147572519-C-T

28386227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 147572521-C-T

28386229-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 147572526-T-G

http://identifiers.org/hco/13/GRCh38#28386455-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147572739-A-C

28386455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 147572739-A-G

http://identifiers.org/hco/13/GRCh38#28386856-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147573062-C-A

28387074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 147573266-A-G

28387075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 147573267-A-G

28387778-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 147573964-T-A

http://identifiers.org/hco/13/GRCh38#28387793-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147573977-A-C

http://identifiers.org/hco/13/GRCh38#28387828-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147573995-C-A

28387828-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 147573995-C-G

28387828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 147573995-C-T

28387935-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 147574121-C-G

28387935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 147574121-C-T

28388008-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 147574180-A-G

28388107-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 147574325-T-A

28388163-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 147574376-A-G

28388242-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 147574455-T-C

28388285-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 147574500-C-G

28388375-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 147574604-G-C

http://identifiers.org/hco/13/GRCh38#28388396-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147574624-C-A

28388396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 147574624-C-T

28388581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 147574804-T-C

http://identifiers.org/hco/13/GRCh38#28388981-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147575207-C-A

28389013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 147575240-G-A

28389013-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 147575240-G-T

28389318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 147575557-A-G

28389389-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 147575639-G-T

28389403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 147575653-T-C

28389403-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 147575653-T-G

http://identifiers.org/hco/13/GRCh38#28389524-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147575767-C-A

28389524-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 147575767-C-T

28389554-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 147575793-C-G

28389554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 147575793-C-T

28389890-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: missense variant
orthologous variants: 147576129-A-T

28390043-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: synonymous variant
orthologous variants: 147576282-T-C

28390150-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147576378-T-A

28390150-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147576378-T-C

28390157-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147576385-A-G

28390184-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147576412-G-T

http://identifiers.org/hco/13/GRCh38#28390191-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147576419-C-A

28390191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147576419-C-T

28390196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147576428-A-G

28390214-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147576446-T-C

http://identifiers.org/hco/13/GRCh38#28390286-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147576530-A-C

28392273-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147578200-A-T

28392380-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147578320-T-C

28392468-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147578418-T-A

28392554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147578503-G-A

28392942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147578881-T-C

28392990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147578951-T-C

28394693-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147580675-C-G

28394693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147580675-C-T

28394695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147580677-C-T

28394848-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147580805-T-C

28394956-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147580883-G-T

28394967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147580894-G-A

28394967-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147580894-G-T

28395004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147580907-C-T

28395111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147580981-G-A

http://identifiers.org/hco/13/GRCh38#28395220-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147581088-C-A

28395322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147581187-C-T

28395565-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147581499-T-C

28396174-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147582136-A-T

28396254-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147582216-A-G

28396477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147582440-C-T

28396671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147582649-G-A

28396860-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147582831-A-T

28396910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147582884-G-A

28396910-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147582884-G-T

28396912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147582886-G-A

28396912-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147582886-G-C

28396912-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147582886-G-T

28396947-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147582918-A-T

28396967-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 147582942-A-G

28397037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 147583012-C-T

28397142-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147583112-T-C

28397142-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147583112-T-G

28397193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147583158-T-C

28397377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147583337-C-T

28397469-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147583426-C-T

28397579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147583520-G-A

28397579-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147583520-G-T

28397716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147583580-T-C

28397796-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147583634-A-G

28398232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147584015-G-A

28398233-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147584016-T-C

28398367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147584115-G-A

28398384-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147584132-A-G

28398467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147584216-C-T

28398642-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147584596-T-G

28398650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147584604-C-T

28398782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147584736-G-A

28398902-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147584862-G-T

28398905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147584865-A-G

http://identifiers.org/hco/13/GRCh38#28398912-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147584872-C-A

http://identifiers.org/hco/13/GRCh38#28398913-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147584873-C-A

28398913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147584873-C-T

http://identifiers.org/hco/13/GRCh38#28398948-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147584910-C-A

28398948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147584910-C-T

28399014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147584975-C-T

http://identifiers.org/hco/13/GRCh38#28399137-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147585098-C-A

28399137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147585098-C-T

28399158-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147585117-C-G

28399158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147585117-C-T

http://identifiers.org/hco/13/GRCh38#28399159-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147585118-C-A

28399159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147585118-C-T

28399173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147585132-G-A

28399173-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147585132-G-T

http://identifiers.org/hco/13/GRCh38#28399184-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147585145-C-A

28399184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147585145-C-T

28399267-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147585225-T-A

28399267-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147585225-T-C

28399345-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147585300-G-T

28399364-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147585344-A-T

28399422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147585396-T-C

28399823-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147586003-T-C

28399939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147586081-C-T

28400058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147586192-G-A

28400529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147586986-G-A

28400564-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147587019-A-G

28400592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147587047-C-T

28400697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147587136-G-A

28400697-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147587136-G-T

28400810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147587250-G-A

28401117-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147587632-T-C

28401878-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147588263-A-G

28401959-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147588326-T-C

28402059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147588423-G-A

28402173-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147588533-A-T

28402204-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147588571-T-C

http://identifiers.org/hco/13/GRCh38#28402321-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147588671-A-C

28402321-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147588671-A-G

28402409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147588757-C-T

http://identifiers.org/hco/13/GRCh38#28402555-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147588895-A-C

28402636-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147588946-A-G

28402683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147588992-G-A

28405205-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147590951-A-G

28405250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147590990-G-A

28405256-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147590996-G-C

28405347-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147591083-T-A

http://identifiers.org/hco/13/GRCh38#28405405-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147591141-C-A

28405416-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147591152-A-G

http://identifiers.org/hco/13/GRCh38#28405639-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147591776-C-A

28405773-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 147591900-A-G

28405942-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147592061-G-T

28405943-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147592062-T-A

28405978-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147592098-G-T

http://identifiers.org/hco/13/GRCh38#28406029-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147592147-A-C

28406029-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147592147-A-G

28406029-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147592147-A-T

28406042-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147592156-T-G

28406170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147592276-A-G

28406188-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147592294-T-C

28406389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147592558-C-T

28406460-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147592637-T-G

28406710-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147592918-A-T

28406771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147592993-G-A

http://identifiers.org/hco/13/GRCh38#28407540-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147593716-C-A

28407804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147593991-G-A

28408142-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147594275-G-A

http://identifiers.org/hco/13/GRCh38#28408255-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147594409-A-C

28408776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147594947-G-A

28408776-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147594947-G-C

28408796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147594967-C-T

28408819-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147594985-T-G

28408964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147595130-C-T

28408992-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147595156-T-C

28409145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147595289-T-C

28409166-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147595307-A-G

28409847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147595891-G-A

28410062-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147596047-T-A

28410092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147596073-C-T

28410211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147596170-C-T

28411970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147596538-C-T

28412047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147596609-G-A

http://identifiers.org/hco/13/GRCh38#28412166-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147596759-C-A

28412167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147596760-A-G

28413010-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147597016-G-T

28413062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147597061-C-T

28413063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147597062-G-A

28413227-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147597246-T-C

28413352-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147597357-C-G

28413355-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147597360-C-G

28413355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147597360-C-T

http://identifiers.org/hco/13/GRCh38#28413518-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147597472-A-C

28413554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147597510-C-T

http://identifiers.org/hco/13/GRCh38#28413699-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147597657-A-C

28413754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147597709-C-T

http://identifiers.org/hco/13/GRCh38#28414416-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147598436-C-A

28414428-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147598448-A-G

28414560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147598558-C-T

28414585-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147598582-T-C

28414601-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147598598-T-C

28414636-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147598620-C-T

28414663-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147598647-A-T

28414678-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147598662-G-T

http://identifiers.org/hco/13/GRCh38#28414850-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147598777-A-C

28414917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147598845-C-T

28415095-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147599020-C-G

28415680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147599279-G-A

28416007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147599597-G-A

28416062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147599655-C-T

28416138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 147599729-C-T

28416383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147599933-C-T

28416535-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147600135-A-T

28416544-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147600148-A-G

28416626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147600227-C-T

http://identifiers.org/hco/13/GRCh38#28416720-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147600317-C-A

28416734-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147600331-T-C

28416803-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147600384-T-C

28416803-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147600384-T-G

28417117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147600618-A-G

http://identifiers.org/hco/13/GRCh38#28417219-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147600717-C-A

http://identifiers.org/hco/13/GRCh38#28417279-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147600780-C-A

28417279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147600780-C-T

28417453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147600938-G-A

28417454-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147600939-T-C

28417994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147601057-C-T

http://identifiers.org/hco/13/GRCh38#28418230-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147601277-C-A

28419000-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147601514-T-C

28419117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147601604-C-T

http://identifiers.org/hco/13/GRCh38#28419532-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147601999-A-C

28419699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147602033-G-A

28420079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147602240-G-A

28420183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147602355-G-A

28420379-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147602548-T-C

28420380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147602549-G-A

28420792-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147602914-T-G

28420833-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147602954-T-C

28420936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147603055-G-A

28421073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147603161-C-T

28421119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147603183-C-T

http://identifiers.org/hco/13/GRCh38#28421910-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147604040-C-A

28421925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147604055-C-T

28422028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147604160-C-T

28422141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147604249-G-A

28423087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147605795-C-T

28423167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147605868-C-T

28423250-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147605952-G-C

28423523-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147606194-T-A

28423523-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147606194-T-C

28424550-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147607245-G-C

28424574-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147607269-T-C

28424762-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147607426-T-A

28424800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147607479-C-T

http://identifiers.org/hco/13/GRCh38#28425330-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147607645-C-A

28425330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147607645-C-T

28425345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147607660-A-G

28425496-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147607818-A-G

28425516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147607829-T-C

28425568-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147607882-G-T

http://identifiers.org/hco/13/GRCh38#28425792-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147608078-C-A

28425792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147608078-C-T

28425793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147608079-G-A

28425832-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147608118-T-C

28426166-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147608452-G-T

28426259-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147608545-C-G

28426259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147608545-C-T

28426547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147608809-G-A

http://identifiers.org/hco/13/GRCh38#28426716-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147608988-A-C

28426781-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147609048-T-A

28426781-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147609048-T-C

28426839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147609105-G-A

28426839-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147609105-G-C

28426966-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147609205-T-G

http://identifiers.org/hco/13/GRCh38#28427045-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147609284-C-A

28427045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147609284-C-T

28427082-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147609310-T-C

28427082-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147609310-T-G

28427138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147609353-A-G

28427138-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147609353-A-T

http://identifiers.org/hco/13/GRCh38#28427144-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147609359-A-C

28427144-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147609359-A-T

28427170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 147609385-A-G

28427170-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 147609385-A-T

28427230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 147609445-G-A

28427230-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 147609445-G-C

http://identifiers.org/hco/13/GRCh38#28427375-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147609587-C-A

28427379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147609591-G-A

28427379-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147609591-G-T

28427398-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147609608-A-T

28427678-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147610273-G-T

28427696-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147610291-T-C

28427804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 147610395-G-A

28427861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 147610452-C-T

28427926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 147610517-G-A

28428541-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147611470-G-C

28428769-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147611858-T-G

28428832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147611901-C-T

28428857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147611918-G-A

28428872-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147611933-A-G

28429185-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147612293-G-C

28429266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147612366-G-A

28429370-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147612470-T-C

28429669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147612782-C-T

http://identifiers.org/hco/13/GRCh38#28429901-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147613002-C-A

28429901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147613002-C-T

http://identifiers.org/hco/13/GRCh38#28429975-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147613057-C-A

28429975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147613057-C-T

28429992-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147613074-G-T

28430028-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147613109-A-G

28430043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 147613124-G-A

28430043-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 147613124-G-T

28430067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 147613148-G-A

28430240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147613321-G-A

28430240-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147613321-G-T

28430252-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147613333-T-C

28430298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147613369-G-A

28430308-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147613379-G-T

28430460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147613487-G-A

28430992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147614800-G-A

28430996-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147614804-A-G

28431058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147614879-C-T

28431059-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147614880-T-A

28431059-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147614880-T-C

28431069-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147614895-A-G

28431069-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147614895-A-T

28431113-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147614935-T-C

28431120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147614942-G-A

28431120-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147614942-G-T

28431275-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 147615093-G-T

28431297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 147615115-G-A

28431314-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 147615132-G-C

28431314-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 147615132-G-T

28431356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147615174-G-A

28431356-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147615174-G-T

28431363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147615181-G-A

28431363-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147615181-G-T

28431369-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147615187-T-A

28431369-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147615187-T-C

http://identifiers.org/hco/13/GRCh38#28431430-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147615656-C-A

28431687-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147615912-T-C

28432004-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147616174-T-C

28432224-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147616347-T-C

28432337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147616451-G-A

http://identifiers.org/hco/13/GRCh38#28432384-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147616500-C-A

http://identifiers.org/hco/13/GRCh38#28432566-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147616689-A-C

28432612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147616739-G-A

28432815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147617423-C-T

28433111-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147617692-T-C

28433231-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147617812-T-G

28433528-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147618124-G-C

28433781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147618382-A-G

http://identifiers.org/hco/13/GRCh38#28433852-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147618457-C-A

28433852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 147618457-C-T

28433873-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 147618478-A-G

28433945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 147618550-G-A

28433984-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147618592-A-G

28433984-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147618592-A-T

28434007-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147618605-A-G

28434098-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 147618695-A-G

http://identifiers.org/hco/13/GRCh38#28434140-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147618737-C-A

28434140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 147618737-C-T

28434179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 147618776-G-A

28434179-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 147618776-G-T

http://identifiers.org/hco/13/GRCh38#28434236-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147618834-C-A

28434247-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147618845-A-G

28434255-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147618855-A-G

http://identifiers.org/hco/13/GRCh38#28434287-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147618877-C-A

28434287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147618877-C-T

28434292-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147618882-T-C

28434358-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147618923-A-G

28434516-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147619086-C-G

28437058-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147619330-A-G

28437090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147619360-G-A

28437149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147619412-C-T

28437201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147619449-T-C

28437312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147619525-C-T

28437682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147619795-C-T

28437683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147619796-G-A

28438005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147620394-G-A

28438069-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147620464-A-G

http://identifiers.org/hco/13/GRCh38#28438100-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147620496-A-C

28438100-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147620496-A-G

28438107-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147620503-A-G

28438107-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147620503-A-T

28438155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147620544-C-T

28438172-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147620577-T-C

28438172-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147620577-T-G

28438175-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147620580-T-G

28438197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147620603-G-A

28438197-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147620603-G-T

28438288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 147620694-G-A

28438317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 147620723-G-A

28438341-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 147620747-T-C

28438351-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 147620757-T-A

28438353-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 147620759-A-G

28438364-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147620767-A-G

28438365-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147620768-A-G

28438397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147620805-G-A

28438397-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147620805-G-T

http://identifiers.org/hco/13/GRCh38#28438437-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147620842-C-A

28438437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147620842-C-T

http://identifiers.org/hco/13/GRCh38#28438444-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147620849-C-A

28438478-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147620881-A-G

http://identifiers.org/hco/13/GRCh38#28438621-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147621007-C-A

28438738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147621106-C-T

28438898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147621245-A-G

28439084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147621375-G-A

28439118-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147621401-T-G

28441915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147622470-G-A

28441953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147622508-T-C

http://identifiers.org/hco/13/GRCh38#28441967-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147622522-A-C

28441990-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147622544-G-C

28442116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147622652-G-A

28442176-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147622705-T-G

http://identifiers.org/hco/13/GRCh38#28442245-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147622765-C-A

28442350-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147622864-G-T

28442360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147622878-C-T

28442362-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147622880-A-G

28442398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147622917-C-T

28442487-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147622993-G-C

28442542-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147623044-A-G

28442556-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147623058-T-C

28443203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147623203-G-A

28443203-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147623203-G-T

28443274-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147623251-C-G

28443323-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147623335-T-C

28443368-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147623377-G-C

28443410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147623410-C-T

28443533-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147623553-T-G

28443717-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147623737-A-G

28443982-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147624230-T-C

28444013-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147624260-A-G

28444147-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147624399-A-G

28444451-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147624616-T-A

28444451-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147624616-T-C

28444609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147624755-C-T

28447972-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147625881-A-G

28448084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147625992-G-A

28448207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147626118-C-T

28448311-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147626221-G-T

28448344-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147626428-G-T

28448576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147626620-G-A

28448787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147626754-G-A

28448787-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147626754-G-C

http://identifiers.org/hco/13/GRCh38#28448935-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147626844-C-A

28448935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147626844-C-T

28448972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147626880-C-T

28449339-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147626921-C-G

28449339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147626921-C-T

28449416-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147626999-T-A

28449685-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147627757-T-C

28450134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147628158-G-A

28450149-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147628170-C-G

28450218-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147628232-T-C

http://identifiers.org/hco/13/GRCh38#28450315-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147628341-C-A

28450410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147628403-G-A

28450410-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147628403-G-C

28450426-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147628419-T-C

28450520-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147628478-G-T

28450537-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147628495-G-C

28450699-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147628569-T-C

28450744-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147628614-G-C

28450755-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147628624-T-C

28450915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147628782-G-A

28450915-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147628782-G-T

http://identifiers.org/hco/13/GRCh38#28450959-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147628827-A-C

28457164-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147631404-A-G

28457294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147631628-C-T

http://identifiers.org/hco/13/GRCh38#28457301-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147631640-C-A

28457301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147631640-C-T

28457554-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147631866-A-G

28457648-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147631958-T-C

28457747-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147632059-C-G

28458258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147632374-C-T

28458655-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147632712-A-G

28458720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147632782-G-A

28458739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147632801-G-A

28458813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147632863-C-T

28458828-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147632878-A-G

28458869-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147632881-T-A

28458869-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147632881-T-C

28458908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147632920-G-A

28459131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147633113-G-A

28459228-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147633206-A-G

28459322-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147633265-G-T

28459332-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147633271-G-T

http://identifiers.org/hco/13/GRCh38#28462244-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147633396-C-A

28462265-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147633416-A-G

28462298-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147633429-T-C

28462362-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147633482-T-C

28462388-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147633508-A-G

28462903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147633942-C-T

28463028-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147634060-A-G

http://identifiers.org/hco/13/GRCh38#28463127-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147634155-A-C

http://identifiers.org/hco/13/GRCh38#28463227-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147634256-C-A

28463268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 147634297-G-A

28463271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 147634300-G-A

28463342-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147634365-G-T

28463395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147634414-A-G

http://identifiers.org/hco/13/GRCh38#28463398-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147634417-C-A

http://identifiers.org/hco/13/GRCh38#28463431-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147634449-C-A

28465480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147635167-C-T

28466083-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147635472-C-G

28466203-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147635595-T-C

28466241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147635626-A-G

28466347-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147635688-T-C

28466420-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147635754-A-G

28466548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147636236-G-A

http://identifiers.org/hco/13/GRCh38#28466599-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147636287-C-A

http://identifiers.org/hco/13/GRCh38#28466640-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147636325-C-A

28466737-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147636414-G-T

28466745-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147636422-T-C

28466796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147636492-G-A

28466796-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147636492-G-T

28466846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147636544-A-G

28466883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147636572-G-A

28467029-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 147636718-A-G

28467168-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147636858-T-C

http://identifiers.org/hco/13/GRCh38#28467182-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147636871-A-C

28467182-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147636871-A-G

28467182-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147636871-A-T

http://identifiers.org/hco/13/GRCh38#28467186-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147636875-C-A

28467186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147636875-C-T

28467213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147636902-G-A

28467213-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147636902-G-T

28467271-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147636937-T-C

28467271-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147636937-T-G

28467383-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147637026-T-C

http://identifiers.org/hco/13/GRCh38#28467430-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147637048-C-A

28467430-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147637048-C-G

28467436-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147637054-G-T

28467438-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147637056-T-C

28467443-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147637058-A-T

28467455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147637067-T-C

28467456-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147637068-G-T

28467477-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147637089-A-G

28467477-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147637089-A-T

28467552-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 147637162-G-T

28467693-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147637291-G-C

28467693-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147637291-G-T

28467701-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147637299-T-C

28467897-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147637469-T-C

28468056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147637715-G-A

28468098-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147637844-G-A

28468217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147637970-G-A

28468225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147637978-G-A

28468257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147638038-C-T

28468260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147638041-T-C

28470983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147639704-G-A

http://identifiers.org/hco/13/GRCh38#28471000-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147639721-A-C

28471000-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147639721-A-G

28472702-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147641817-A-T

28472859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147642083-C-T

28473131-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147642348-G-T

28473154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147642370-G-A

28475599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147643801-G-A

http://identifiers.org/hco/13/GRCh38#28475898-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147644053-C-A

28475955-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147644107-G-T

28476030-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147644186-A-G

28476262-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147644407-T-A

28476262-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147644407-T-G

28476717-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147644868-T-A

28477007-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147645282-C-G

28477022-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147645297-T-A

28477099-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147645339-C-G

28477099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147645339-C-T

http://identifiers.org/hco/13/GRCh38#28477446-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147645678-C-A

28477539-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 147645750-T-C

http://identifiers.org/hco/13/GRCh38#28477599-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147645806-C-A

28477638-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147645839-T-C

28477904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147646087-C-T

http://identifiers.org/hco/13/GRCh38#28480788-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147648018-A-C

28480850-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147648055-G-T

28480855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147648060-C-T

28481102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147648284-G-A

28481185-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147648340-C-G

28481227-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147648380-T-C

28481442-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147648542-T-A

28481442-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147648542-T-C

28481592-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147648748-T-G

28481735-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147648894-G-T

28481756-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147648915-G-C

28481760-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147648919-A-G

http://identifiers.org/hco/13/GRCh38#28481761-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147648920-C-A

28482307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147649372-G-A

28482582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147649539-T-C

28483027-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147649946-T-G

28483122-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147650042-G-T

28483225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147650143-T-C

28483471-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147650446-A-T

http://identifiers.org/hco/13/GRCh38#28483931-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147651675-A-C

28484058-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147651792-G-T

http://identifiers.org/hco/13/GRCh38#28484199-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147651936-C-A

28484199-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147651936-C-G

http://identifiers.org/hco/13/GRCh38#28484495-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147652177-A-C

28485428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147653362-C-T

28485778-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147653652-T-C

28485821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147653694-G-A

28485821-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147653694-G-T

28485859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147653728-G-A

28485891-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147653760-C-G

28486047-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147653911-G-C

28486072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147653931-C-T

28486190-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147654015-T-C

28486406-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147654183-G-T

28486417-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147654194-C-G

28486417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147654194-C-T

28486578-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147654363-C-G

28486715-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147654526-A-G

28486803-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147654616-C-G

28486907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147654727-G-A

28487166-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147654976-T-C

28487410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147655219-C-T

28487419-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147655228-C-G

28487550-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147655353-C-G

28487550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147655353-C-T

28487618-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147655426-T-C

28487740-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147655542-G-C

http://identifiers.org/hco/13/GRCh38#28488061-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147655830-C-A

28488414-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147655881-G-T

28490028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147658041-G-A

28490029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147658042-G-A

28490088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147658101-G-A

28490091-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147658106-C-G

28490317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147658313-G-A

28490443-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147658461-C-G

28490638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147658651-C-T

28491164-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147659106-T-C

28491432-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147659401-G-C

28491678-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147659666-T-C

28491854-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147659954-A-T

28492316-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147660577-A-G

28493712-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147661508-C-G

28493818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147661609-C-T

28493831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147661622-C-T

28494537-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147662289-C-T

28494606-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147662347-G-T

28494647-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147662395-T-G

http://identifiers.org/hco/13/GRCh38#28494759-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147662460-C-A

28494759-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147662460-C-G

28494759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 147662460-C-T

http://identifiers.org/hco/13/GRCh38#28494864-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147662565-C-A

28494864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: 5 prime UTR variant
orthologous variants: 147662565-C-T

28494908-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: 5 prime UTR variant
orthologous variants: 147662609-A-G

28494908-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: 5 prime UTR variant
orthologous variants: 147662609-A-T

http://identifiers.org/hco/13/GRCh38#28494920-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#147662621-C-A

28494920-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: 5 prime UTR variant
orthologous variants: 147662621-C-G

28494920-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: 5 prime UTR variant
orthologous variants: 147662621-C-T

28495083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: 5 prime UTR variant
orthologous variants: 147662777-G-A

28495083-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: 5 prime UTR variant
orthologous variants: 147662777-G-C

28495083-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: 5 prime UTR variant
orthologous variants: 147662777-G-T

http://identifiers.org/hco/13/GRCh38#28495107-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#147662800-C-A

28495107-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 147662800-C-G

28495107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 147662800-C-T

28495129-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: 5 prime UTR variant
orthologous variants: 147662822-G-T

28495130-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3763
most severe consequence: 5 prime UTR variant
orthologous variants: 147662823-A-G