http://identifiers.org/hco/10/GRCh38#129835482-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#136795650-C-A

129835485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 136795653-G-A

129835485-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 136795653-G-C

129835485-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 136795653-G-T

http://identifiers.org/hco/10/GRCh38#129835612-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#136795766-C-A

129835793-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 136795955-G-T

129835804-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 136795966-G-T

129835848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 136796002-G-A

129835947-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 136796103-C-G

129836060-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 136796207-A-G

129836060-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 136796207-A-T

129836105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 136796249-G-A

129836105-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 136796249-G-T

129836448-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 136796620-C-G

129836477-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 136796649-G-T

http://identifiers.org/hco/10/GRCh38#129836591-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#136796763-C-A

129837370-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136797542-T-A

129837370-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136797542-T-C

129837404-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136797576-T-C

http://identifiers.org/hco/10/GRCh38#129837409-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#136797581-A-C

129837533-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136797702-G-T

http://identifiers.org/hco/10/GRCh38#129837870-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#136798043-C-A

129837870-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136798043-C-G

129837870-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136798043-C-T

129837915-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136798087-T-C

129837938-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 136798109-C-G

129837938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 136798109-C-T

129837949-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 136798120-G-T

129838060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136798224-G-A

http://identifiers.org/hco/10/GRCh38#129838076-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#136798240-C-A

129838076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136798240-C-T

129838098-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136798264-G-A

129838098-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136798264-G-T

129838135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136798305-G-A

129838146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136798316-C-T

129838476-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136798573-C-G

129838897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136798979-C-T

129838914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136798994-G-A

http://identifiers.org/hco/10/GRCh38#129839000-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#136799080-C-A

129839000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136799080-C-T

http://identifiers.org/hco/10/GRCh38#129839288-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#136799365-C-A

129839333-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136799410-A-T

129839418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136799492-A-G

129839523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136799609-C-T

129839785-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136799848-A-G

129839880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136799941-G-A

129839880-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136799941-G-T

http://identifiers.org/hco/10/GRCh38#129839908-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#136799963-C-A

129839908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136799963-C-T

129840102-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136800111-A-G

http://identifiers.org/hco/10/GRCh38#129840230-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#136800206-C-A

129840230-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136800206-C-G

129840230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136800206-C-T

129840234-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136800210-A-G

129840493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136800470-G-A

129840602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136800570-G-A

http://identifiers.org/hco/10/GRCh38#129840679-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#136800658-C-A

129840713-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136800692-C-G

129840713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136800692-C-T

129841148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136801131-C-T

129841229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136801202-C-T

129841739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136801741-C-T

http://identifiers.org/hco/10/GRCh38#129842096-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#136802092-C-A

129842215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 136802211-G-A

129842215-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 136802211-G-C

129842746-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136802534-A-G

http://identifiers.org/hco/10/GRCh38#129842761-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#136802549-C-A

129842761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136802549-C-T

129842987-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136802756-A-G

129843020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136802762-G-A

129843020-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136802762-G-C

129843020-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136802762-G-T

http://identifiers.org/hco/10/GRCh38#129843055-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#136802795-A-C

129843176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 136802894-G-A

129843176-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 136802894-G-C

129843280-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136802992-T-C

http://identifiers.org/hco/10/GRCh38#129843307-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#136803020-A-C

129843307-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136803020-A-G

129843445-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136803142-G-T

129843455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136803152-G-A

129843455-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136803152-G-T

129843506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136803201-G-A

129843857-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136803550-A-T

129843914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136803598-G-A

129844027-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136803712-A-G

129844109-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136803776-A-T

129844134-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136803800-G-C

http://identifiers.org/hco/10/GRCh38#129844153-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#136803807-C-A

129844269-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136803881-T-A

129844436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136804051-G-A

129844485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136804097-G-A

129844552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136804164-C-T

http://identifiers.org/hco/10/GRCh38#129845240-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#136804852-C-A

129845240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136804852-C-T

129845926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136805543-T-C

http://identifiers.org/hco/10/GRCh38#129845967-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#136805584-C-A

129845967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136805584-C-T

http://identifiers.org/hco/10/GRCh38#129846012-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#136805629-C-A

129846036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136805653-C-T

129846062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136805679-G-A

129846400-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136805986-T-C

129846528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136806110-C-T

129846568-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136806150-T-C

129846768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136806350-C-T

129846794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136806376-G-A

129847031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136806631-C-T

129847057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136806658-C-T

129847142-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136806705-G-A

129847250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136806815-A-G

129847277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136806845-C-T

http://identifiers.org/hco/10/GRCh38#129847348-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#136806912-A-C

129848251-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136807770-T-A

129848314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136807832-G-A

129848314-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136807832-G-C

129848314-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136807832-G-T

http://identifiers.org/hco/10/GRCh38#129848321-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#136807843-C-A

129848321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136807843-C-T

129848520-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136808046-T-G

129848600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136808123-C-T

129848734-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136808262-T-C

129849499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136809014-C-T

129850249-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136809765-T-C

129850353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136809866-C-T

129850388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136809901-T-C

129850419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136809930-G-A

129850533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136810047-G-A

129850542-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136810056-G-C

129850663-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136810182-A-T

129850977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136810461-G-A

129850977-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136810461-G-T

129852352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136811819-T-C

129852390-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136811857-T-C

129852685-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136812149-T-C

129852891-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136812361-A-G

129853194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136812648-C-T

129853236-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136812689-T-A

129853562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136812993-G-A

129854037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136813467-G-A

129854062-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136813492-C-G

129854062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136813492-C-T

129854066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136813504-C-T

129854478-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136813927-A-T

129854872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136814321-C-T

129854873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136814322-G-A

129854931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136814367-G-A

129855034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136814467-C-T

129855477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136814889-C-T

129855531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136814946-G-A

129855734-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136815116-T-C

129855933-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136815299-A-G

129856306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136815601-G-A

129856319-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136815611-A-G

129856413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136815705-C-T

129857282-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136816925-C-G

129857672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136818228-G-A

129857811-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136818340-T-A

129857909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136818454-G-A

129858471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136818933-G-A

129858471-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136818933-G-T

http://identifiers.org/hco/10/GRCh38#129858502-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#136818961-C-A

129858529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136818982-C-T

129858988-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136819471-A-G

http://identifiers.org/hco/10/GRCh38#129858999-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#136819482-C-A

129858999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136819482-C-T

129859601-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136819749-A-G

129859834-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136819969-G-A

129859834-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136819969-G-C

129859903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136820027-G-A

129860304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136820362-G-A

129860443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136820489-C-T

129860444-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136820490-A-T

129860565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136820607-G-A

129860565-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136820607-G-T

129860615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136820657-C-T

129861085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136821106-C-T

129861254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136821242-C-T

129861302-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136821278-C-G

129861517-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136821507-A-G

129861669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136821651-C-T

http://identifiers.org/hco/10/GRCh38#129861675-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#136821658-C-A

129861675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136821658-C-T

129861753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136821726-C-T

129861924-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136821944-G-A

129862019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136822037-G-A

129862103-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136822147-A-G

129862122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136822167-C-T

129862299-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136822322-T-C

129862536-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136822545-G-C

129863503-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136823542-T-A

129863875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136823972-G-A

129863875-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136823972-G-T

129864394-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136824414-A-G

129864488-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136824522-A-G

129864488-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136824522-A-T

129864492-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136824526-A-G

129864492-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136824526-A-T

129864603-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136824645-C-G

129864603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136824645-C-T

129864747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136824786-G-A

129864750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136824788-C-T

129864775-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136824811-A-T

129864854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136824882-C-T

129864903-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136824933-C-G

129864936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136824965-G-A

129865004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136825030-G-A

129865020-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136825058-C-G

129865020-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136825058-C-T

129865483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136825500-C-T

129865677-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136825755-T-C

129865696-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136825786-G-T

129865839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136825929-G-A

129865960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136826032-C-T

129866053-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136826118-T-C

129866174-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136826182-T-G

129866630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136826401-C-T

129866903-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136826652-A-G

129867013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136826754-G-A

129867013-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136826754-G-T

http://identifiers.org/hco/10/GRCh38#129867049-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#136826778-C-A

129867049-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136826778-C-G

129867051-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136826780-C-G

129867061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136826790-C-T

129867066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136826795-G-A

129867066-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136826795-G-C

129867094-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136826826-A-G

http://identifiers.org/hco/10/GRCh38#129867101-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#136826832-C-A

129867101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136826832-C-T

129867102-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136826833-T-C

129867217-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 136826948-A-G

129867301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136827031-G-A

129867320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136827050-G-A

129867377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136827106-G-A

129867377-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136827106-G-T

129867598-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136827323-G-T

129867606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136827331-G-A

129867606-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136827331-G-T

http://identifiers.org/hco/10/GRCh38#129867916-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#136827619-C-A

129867916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 136827619-C-T

129868005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136827707-G-A

129868008-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136827710-G-C

http://identifiers.org/hco/10/GRCh38#129868050-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#136827750-C-A

129868050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136827750-C-T

129868051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136827751-G-A

129868051-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136827751-G-T

http://identifiers.org/hco/10/GRCh38#129868058-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#136827758-A-C

129868171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136827877-C-T

129868644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136828325-G-A

129868660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136828338-G-A

129868765-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136828437-T-C

129869077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136828728-C-T

129869085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136828736-A-G

129869371-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136828997-T-A

129869389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136829017-C-T

http://identifiers.org/hco/10/GRCh38#129869429-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#136829037-A-C

129869430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136829038-C-T

129869431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136829039-G-A

129869431-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136829039-G-C

129869469-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136829074-C-T

129870482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136830082-G-A

129870538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136830137-G-A

http://identifiers.org/hco/10/GRCh38#129870574-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#136830168-C-A

129870811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136830287-C-T

129870819-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136830295-T-C

129870819-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136830295-T-G

129871095-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136830574-C-G

129871095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136830574-C-T

129871608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136831094-G-A

129871751-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136831253-C-G

129871951-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136831454-G-C

129871973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136831474-A-G

129872519-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136832018-T-A

129872817-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136832267-A-G

129873216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136832648-C-T

129873380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136832813-G-A

129873380-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136832813-G-T

129873425-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136832861-A-G

http://identifiers.org/hco/10/GRCh38#129873647-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#136833099-C-A

129873647-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136833099-C-G

129873647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136833099-C-T

129873702-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136833148-T-C

129873745-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136833226-T-A

http://identifiers.org/hco/10/GRCh38#129874163-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#136833663-C-A

129874233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136833721-G-A

129874279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136833735-G-A

129874279-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136833735-G-T

129874668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136834054-G-A

http://identifiers.org/hco/10/GRCh38#129874792-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#136834105-C-A

129874792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136834105-C-T

129874861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136834183-C-T

129874876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136834198-C-T

129874967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136834272-C-T

129874995-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136834302-T-C

129875017-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136834320-T-A

129875030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136834333-C-T

129875827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136835932-G-A

http://identifiers.org/hco/10/GRCh38#129876016-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#136836082-A-C

129876199-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136836237-T-C

129876225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136836267-G-A

129876252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136836294-G-A

129876446-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136836465-T-C

129876988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136836907-T-C

129877036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136836941-G-A

129877045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136836951-C-T

http://identifiers.org/hco/10/GRCh38#129877297-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#136837205-C-A

129877708-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136837578-A-G

129877709-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136837579-A-G

129877716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136837589-T-C

129877716-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136837589-T-G

129877722-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136837595-A-T

http://identifiers.org/hco/10/GRCh38#129877737-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#136837605-C-A

129877737-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136837605-C-G

129877739-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136837607-C-G

129877739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136837607-C-T

http://identifiers.org/hco/10/GRCh38#129877954-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#136837810-C-A

129877954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 136837810-C-T

129878206-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136838052-T-C

129878307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136838154-C-T

129878687-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136838339-T-A

129878687-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136838339-T-C

129878687-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136838339-T-G

129878946-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136838474-G-C

129879423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136838922-G-A

129879762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136839252-G-A

129879946-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136839434-C-G

129879946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136839434-C-T

129879947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136839435-G-A

129879979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136839467-G-A

129880168-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136839647-A-G

http://identifiers.org/hco/10/GRCh38#129880176-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#136839654-A-C

129880629-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136839869-C-T

129880931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136840099-G-A

129880997-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136840163-T-C

129881001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136840167-G-A

129881104-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136840272-C-G

129881472-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136840642-T-C

129881485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136840655-G-A

129881485-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136840655-G-C

http://identifiers.org/hco/10/GRCh38#129881512-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#136840677-C-A

129881512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136840677-C-T

129881722-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136840846-T-G

129881727-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136840851-A-G

129881761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136840890-G-A

129881761-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136840890-G-C

129882036-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136841139-T-A

129882036-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136841139-T-G

129882046-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136841149-T-C

129882759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136841866-G-A

129882980-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136842082-T-A

129882993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136842095-C-T

129883112-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136842241-A-G

129883112-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136842241-A-T

129883243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136842377-C-T

129883324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136842453-C-T

129883430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136842554-G-A

129883452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136842573-G-A

129883452-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136842573-G-T

129883528-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136842644-C-G

129883528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136842644-C-T

129883728-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136842862-T-G

129883742-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136842874-T-G

129883773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136842906-G-A

129883773-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136842906-G-C

129883773-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136842906-G-T

129883964-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136843086-A-G

129883973-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136843095-T-C

http://identifiers.org/hco/10/GRCh38#129884598-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#136843715-C-A

129884598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136843715-C-T

129884662-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136843785-T-C

http://identifiers.org/hco/10/GRCh38#129885036-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#136844169-A-C

129885688-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136844815-G-T

129885864-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136844989-T-G

129886781-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136845863-T-C

129886916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136846027-C-T

http://identifiers.org/hco/10/GRCh38#129886997-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#136846128-C-A

129887029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136846158-G-A

129887069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136846170-G-A

129887135-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136846215-T-C

129887200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136846280-C-T

129887352-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136846432-C-G

129887352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136846432-C-T

129887992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136847109-G-A

129888149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136847244-G-A

129888149-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136847244-G-C

129888149-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136847244-G-T

129888205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136847298-C-T

129888320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136847414-T-C

129888439-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136847529-T-C

129888556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136847643-G-A

129888595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136847681-C-T

129889037-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136848123-G-C

129889216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 136848324-C-T

129889441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136848554-C-T

129889444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136848557-C-T

129889536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136848650-G-A

129889577-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136848700-T-A

129889730-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136848849-G-C

http://identifiers.org/hco/10/GRCh38#129889856-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#136848923-C-A

129889949-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136848995-T-A

129889972-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136849030-T-C

129889972-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136849030-T-G

129890472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136849508-C-T

129891526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136850560-C-T

129891661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136850698-C-T

129891868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136850870-G-A

129891898-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136850900-G-C

129892027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136851030-G-A

129892230-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136851237-A-G

129892271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136851282-C-T

129892414-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136851414-C-G

129892414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136851414-C-T

129892810-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136851773-C-G

129893442-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136852403-T-G

129893840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136852788-C-T

129893841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136852789-G-A

129893907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136852836-G-A

129894082-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136853013-A-G

129894319-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136853244-G-C

129894500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136853453-G-A

http://identifiers.org/hco/10/GRCh38#129894513-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#136853469-C-A

129894813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136853716-G-A

129894963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136853862-C-T

129895082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136853971-C-T

129895414-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136854226-G-T

129895519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136854306-C-T

129895673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136854454-C-T

129896417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 136855219-C-T

129896425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 136855227-C-T

129896433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 136855236-G-A

129896530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 136855357-G-A

129896605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136855432-G-A

129896615-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136855460-C-G

129896615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136855460-C-T

129897129-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136855978-G-C

129897246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136856048-G-A

129897329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136856118-G-A

129897482-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136856267-T-C

129897890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136856672-G-A

129897990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136856772-G-A

129898880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136857622-G-A

129899221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136857966-G-A

129899227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136857972-G-A

129899227-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136857972-G-C

129899266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136858009-C-T

129899528-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136858271-C-G

129899767-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136858495-C-G

129899767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136858495-C-T

129899780-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136858508-A-G

129899812-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136858535-T-C

129899954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136858677-G-A

129900266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136858989-G-A

129900556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136859256-A-G

129900565-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136859263-G-T

129900694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136859366-G-A

http://identifiers.org/hco/10/GRCh38#129900754-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#136859414-A-C

129900935-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136859647-T-C

http://identifiers.org/hco/10/GRCh38#129901065-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#136859825-A-C

129901065-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136859825-A-G

129901422-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136860185-G-C

129901894-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136860656-T-G

http://identifiers.org/hco/10/GRCh38#129901985-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#136860745-C-A

129902104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136860843-G-A

129902145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136860884-G-A

129902407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136861178-G-A

129902407-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136861178-G-T

129902450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136861210-C-T

129902466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136861225-G-A

http://identifiers.org/hco/10/GRCh38#129902542-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#136861305-A-C

129902768-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136861485-A-T

129903308-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136861955-T-G

129903645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136862239-G-A

129903840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136862832-C-T

129903993-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136862926-C-G

129904060-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136862968-C-G

http://identifiers.org/hco/10/GRCh38#129904292-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#136863111-C-A

129904527-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136863247-G-T

129905067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136863621-C-T

129905085-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136863639-C-G

http://identifiers.org/hco/10/GRCh38#129905160-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#136863718-A-C

129905160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136863718-A-G

129905165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136863723-G-A

http://identifiers.org/hco/10/GRCh38#129905274-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#136863833-C-A

129905277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136863836-G-A

http://identifiers.org/hco/10/GRCh38#129905377-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#136863947-A-C

129905465-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136864027-G-C

129905465-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136864027-G-T

129905561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136864100-G-A

129906403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136864909-G-A

129906931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136865428-C-T

129907352-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136865848-C-G

129907584-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136866081-C-G

129907584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136866081-C-T

129908452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136866949-G-A

129908498-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136866995-C-G

http://identifiers.org/hco/10/GRCh38#129908594-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#136867084-C-A

129908594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136867084-C-T

129908628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136867120-G-A

129908679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136867171-C-T

129908910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136867399-C-T

129909223-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136867707-T-A

129909223-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136867707-T-C

129909328-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136867791-C-G

129909387-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136867849-T-C

129909564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136868024-G-A

129909564-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136868024-G-C

129909760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136868219-C-T

129909986-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136868442-G-C

129910001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136868457-C-T

129910415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136868867-A-G

129910471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136868922-C-T

129910575-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136869026-T-C

129910656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136869102-C-T

129910761-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136869215-T-C

129911024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136869480-G-A

129911097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136869556-G-A

129911592-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136870031-G-C

129911842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136870263-G-A

129911842-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136870263-G-C

129912213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136870592-G-A

129914289-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136872687-T-C

129914520-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136872917-C-G

129915370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136873840-C-T

129915638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136874083-G-A

129916227-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136874614-C-G

129916418-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136874838-C-G

129916486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136874948-C-T

129916487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136874949-G-A

129916548-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136875070-G-C

129916741-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136875269-T-C

129916945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136875448-G-A

129917055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136875548-G-A

129917055-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136875548-G-C

129917934-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136876258-T-C

129918051-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136876335-C-G

129918062-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136876342-T-C

129918121-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136876389-C-G

http://identifiers.org/hco/10/GRCh38#129918287-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#136876542-A-C

http://identifiers.org/hco/10/GRCh38#129918292-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#136876548-C-A

129918292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136876548-C-T

129918318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136876569-C-T

129918386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136876633-C-T

129918573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136876799-C-T

129918618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136876845-C-T

129919298-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136877796-G-T

129919543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136877998-A-G

129919555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136878010-A-G

129920526-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136878271-C-G

129920617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136878357-C-T

129920623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136878363-G-A

129920725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136878432-C-T

129920738-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136878445-T-C

129920787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136878479-C-T

129920840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136878527-G-A

129920985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136878661-C-T

129921118-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136878786-G-C

129921151-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136878809-T-G

129921306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136878896-C-T

129921307-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136878897-A-G

129921482-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136879061-T-C

http://identifiers.org/hco/10/GRCh38#129921862-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#136879355-A-C

129921989-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136879454-C-G

http://identifiers.org/hco/10/GRCh38#129922126-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#136879619-C-A

http://identifiers.org/hco/10/GRCh38#129922171-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#136879653-C-A

129922171-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136879653-C-G

129922184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136879666-C-T

129922432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136879912-C-T

129922442-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136879921-T-C

http://identifiers.org/hco/10/GRCh38#129922705-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#136880138-C-A

129922705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136880138-C-T

129922768-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136880197-T-C

129922791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136880218-C-T

http://identifiers.org/hco/10/GRCh38#129922802-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#136880242-C-A

129926234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136883345-G-A

129926237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136883348-G-A

http://identifiers.org/hco/10/GRCh38#129926240-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#136883351-C-A

129926254-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136883363-C-G

129926254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136883363-C-T

129926255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136883364-G-A

129926274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136883381-C-T

129926399-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136883489-C-G

129926435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136883516-G-A

129927345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136884968-A-G

129927415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136885039-A-G

129927580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136885153-C-T

129927598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136885171-G-A

129927598-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136885171-G-C

129927605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136885178-A-G

129927925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136885488-G-A

129927980-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136885546-G-C

129928042-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136885600-G-T

129928588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136886021-C-T

129928848-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136886208-C-G

129928848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136886208-C-T

129928984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136886327-T-C

129929049-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136886392-G-C

129929173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136886511-G-A

129929584-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136886584-T-A

129929584-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136886584-T-C

129929614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136886614-G-A

129929642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136886641-C-T

129931356-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136886908-G-C

http://identifiers.org/hco/10/GRCh38#129931576-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#136887116-C-A

129931576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136887116-C-T

129931619-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136887148-A-G

http://identifiers.org/hco/10/GRCh38#129931801-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#136887335-C-A

129931801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136887335-C-T

129931829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136887362-A-G

129931863-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136887400-G-C

129931875-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136887412-G-T

129931886-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136887421-G-T

129932339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136887904-C-T

129932540-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136888117-T-A

129932776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136888339-C-T

129933124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136888706-T-C

129933218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136888808-A-G

129933388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136888991-C-T

129933646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136889229-G-A

http://identifiers.org/hco/10/GRCh38#129933827-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#136889331-A-C

129933858-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136889353-G-A

129933858-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136889353-G-C

129933864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136889358-C-T

129933990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136889495-T-C

129934268-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136889824-A-G

129934275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136889831-T-C

http://identifiers.org/hco/10/GRCh38#129934308-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#136889874-C-A

129934349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136889915-A-G

129934616-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136890175-G-C

129935075-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136890614-C-G

129935632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136890906-T-C

129935693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136890950-G-A

129935830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136891066-G-A

http://identifiers.org/hco/10/GRCh38#129935859-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#136891096-C-A

129935953-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136891189-A-T

129935957-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136891201-A-G

129939567-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136892905-A-T

129939825-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136893165-T-C

129940089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136893475-C-T

129940327-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136893713-T-C

129940575-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136893900-A-G

129940724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136894039-G-A

http://identifiers.org/hco/10/GRCh38#129940929-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#136894222-C-A

http://identifiers.org/hco/10/GRCh38#129940980-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#136894270-C-A

129940980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136894270-C-T

129941058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136894343-G-A

129941058-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136894343-G-T

129941198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136894480-C-T

129941585-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136894776-T-C

129941586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136894777-C-T

129941672-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136894848-C-G

129941672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136894848-C-T

129941845-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136894933-T-C

129942021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136894988-G-A

129942131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136895096-C-T

129942260-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136895233-A-G

129942293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136895267-C-T

129942881-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136895770-A-G

129942889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136895778-G-A

129942902-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136895787-T-C

129942928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136895809-G-A

129942977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136895858-G-A

129943401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136896266-T-C

129943587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136896457-C-T

129944644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136897548-C-T

129945016-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136897921-C-G

129945131-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136897993-G-T

129945146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136898008-G-A

129945150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136898012-G-A

129945279-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136898098-T-C

129945402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136898220-C-T

129945437-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136898255-T-C

129945447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136898265-G-A

129945769-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136898587-T-C

129945913-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136898730-G-C

129945997-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136898814-T-A

129945997-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136898814-T-C

129946012-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136898829-T-A

129946012-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136898829-T-C

129946132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136898970-G-A

129946296-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136899134-C-G

129946296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136899134-C-T

129946389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136899226-G-A

129946419-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136899256-A-G

129946422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136899259-T-C

129946529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136899352-G-A

129946529-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136899352-G-T

129946583-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136899404-T-C

129946591-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136899412-G-C

129946625-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136899445-G-C

129946901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136899712-G-A

129946903-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136899714-T-C

129946965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136899771-C-T

129947106-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136899914-A-G

129947144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136899952-A-G

http://identifiers.org/hco/10/GRCh38#129947707-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#136900511-C-A

http://identifiers.org/hco/10/GRCh38#129947919-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#136900684-C-A

129947969-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136900733-A-T

129948392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136900819-G-A

129948392-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136900819-G-C

129948393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136900820-G-A

129948393-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136900820-G-C

129948989-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136901346-G-C

129949368-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136901391-C-G

129949396-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136901421-A-G

129949657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136901632-G-A

http://identifiers.org/hco/10/GRCh38#129949769-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#136901738-C-A

129949769-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136901738-C-T

http://identifiers.org/hco/10/GRCh38#129949880-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#136901830-C-A

129950289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136902198-G-A

129950406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136902307-G-A

129950603-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136902519-C-G

129950804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136902704-G-A

129950899-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136902808-G-C

129951095-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136903008-G-C

129951166-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136903085-C-G

129951166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136903085-C-T

129951249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136903170-C-T

129951489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136903413-C-T

http://identifiers.org/hco/10/GRCh38#129951633-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#136903569-A-C

http://identifiers.org/hco/10/GRCh38#129951694-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#136903633-A-C

129952172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136904101-G-A

129952172-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136904101-G-T

129952595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136904522-G-A

129952702-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136904629-C-G

129952702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136904629-C-T

129953103-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136905025-A-G

129953206-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136905135-T-C

129953387-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136905317-T-G

http://identifiers.org/hco/10/GRCh38#129953406-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#136905336-A-C

129953406-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136905336-A-G

http://identifiers.org/hco/10/GRCh38#129955254-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#136907166-A-C

129955254-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136907166-A-G

129955392-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136907304-A-T

129955621-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136907546-T-C

129955999-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136907959-T-G

129956124-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136908084-T-A

http://identifiers.org/hco/10/GRCh38#129957379-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#136909335-C-A

129957379-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136909335-C-G

129957379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136909335-C-T

http://identifiers.org/hco/10/GRCh38#129958437-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#136910459-A-C

129958437-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136910459-A-G

129958786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136910876-C-T

http://identifiers.org/hco/10/GRCh38#129958788-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#136910878-C-A

129958788-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136910878-C-G

129958788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136910878-C-T

129958847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136910945-G-A

http://identifiers.org/hco/10/GRCh38#129958867-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#136910972-C-A

129958867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136910972-C-T

129958905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136910998-G-A

129958928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136911022-G-A

129958928-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136911022-G-T

129959012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 136911106-G-A

129959014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 136911108-G-A

129959066-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136911160-T-C

129959066-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136911160-T-G

129959082-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136911176-A-G

http://identifiers.org/hco/10/GRCh38#129959127-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#136911224-C-A

129959127-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136911224-C-G

129959127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136911224-C-T

129959162-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136911245-A-G

129959238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136911321-G-A

129959377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136911418-C-T

http://identifiers.org/hco/10/GRCh38#129959787-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#136911759-C-A

129959804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136911776-G-A

129959805-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136911777-G-C

129960151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136912105-C-T

http://identifiers.org/hco/10/GRCh38#129960238-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#136912195-A-C

129960238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136912195-A-G

129960455-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136912401-T-G

129960939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136912880-G-A

129961022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136912956-C-T

129961189-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136913108-G-C

129961655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136913549-G-A

129961723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136913617-G-A

129961781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136913675-C-T

129961944-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136913845-A-G

http://identifiers.org/hco/10/GRCh38#129962060-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#136913962-C-A

129962060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136913962-C-T

http://identifiers.org/hco/10/GRCh38#129962289-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#136914199-C-A

129962289-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136914199-C-G

129962289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136914199-C-T

129962369-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136914264-A-G

129962452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136914340-G-A

129962588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136914463-G-A

129962633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136914508-C-T

129962639-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136914514-T-C

129962720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136914595-C-T

129963058-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136914937-C-G

129963083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136914962-C-T

http://identifiers.org/hco/10/GRCh38#129963093-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#136914973-C-A

129963093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 136914973-C-T

http://identifiers.org/hco/10/GRCh38#129963206-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#136915092-C-A

129963206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136915092-C-T

129963257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 136915141-T-C

129963300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136915182-G-A

129963300-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136915182-G-T

129963879-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: 5 prime UTR variant
orthologous variants: 136915753-C-G

129964189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 136916072-G-A

129964189-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 136916072-G-C

http://identifiers.org/hco/10/GRCh38#129964490-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#136916373-A-C

129964565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron variant
orthologous variants: 136916448-G-A

129964871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron variant
orthologous variants: 136916767-G-A

129964929-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron variant
orthologous variants: 136916825-T-C

129965317-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron variant
orthologous variants: 136917217-G-C

129965391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron variant
orthologous variants: 136917291-G-A

129966092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron variant
orthologous variants: 136917998-G-A

129966908-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron variant
orthologous variants: 136918786-G-C

129967143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron variant
orthologous variants: 136918997-C-T

129967150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron variant
orthologous variants: 136919004-G-A

http://identifiers.org/hco/10/GRCh38#129967177-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#136919031-C-A

129967185-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron variant
orthologous variants: 136919039-A-G

129967607-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron variant
orthologous variants: 136919441-A-G

129967723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron variant
orthologous variants: 136919533-C-T

http://identifiers.org/hco/10/GRCh38#129967794-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#136919583-C-A

129968163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron variant
orthologous variants: 136919934-C-T

129968259-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron variant
orthologous variants: 136920036-T-G

129968388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron variant
orthologous variants: 136920133-G-A

129968430-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron variant
orthologous variants: 136920174-G-T

129968621-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron variant
orthologous variants: 136920331-G-C

129968626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron variant
orthologous variants: 136920336-G-A

129968647-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron variant
orthologous variants: 136920366-G-C

129968949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron variant
orthologous variants: 136920660-C-T

129969061-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron variant
orthologous variants: 136920766-A-G

129969256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron variant
orthologous variants: 136920949-G-A

129970058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron variant
orthologous variants: 136921762-C-T

129970511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron variant
orthologous variants: 136922130-G-A

129970718-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron variant
orthologous variants: 136922311-G-C

129970779-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron variant
orthologous variants: 136922370-T-C

129970863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron variant
orthologous variants: 136922440-C-T

129971524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron variant
orthologous variants: 136923086-G-A

129971524-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron variant
orthologous variants: 136923086-G-C

129971524-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron variant
orthologous variants: 136923086-G-T

129972473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron variant
orthologous variants: 136924055-C-T

129972661-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron variant
orthologous variants: 136924215-C-G

129972846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron variant
orthologous variants: 136924361-G-A

129972846-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19087
most severe consequence: intron variant
orthologous variants: 136924361-G-T