http://identifiers.org/hco/17/GRCh38#75785197-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#115921518-C-A

75785197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115921518-C-T

75785227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115921548-G-A

75785227-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115921548-G-T

http://identifiers.org/hco/17/GRCh38#75785270-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#115921590-A-C

75785270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115921590-A-G

http://identifiers.org/hco/17/GRCh38#75785336-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#115921628-A-C

75785484-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115921768-C-G

75785637-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115921887-G-T

75785817-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115922039-G-T

75786056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 115922243-C-T

75789119-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 115926547-T-C

75791295-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 115928889-T-C

75791497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 115929111-G-A

http://identifiers.org/hco/17/GRCh38#75791631-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#115929237-C-A

http://identifiers.org/hco/17/GRCh38#75791632-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#115929238-C-A

75791632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 115929238-C-T

http://identifiers.org/hco/17/GRCh38#75791650-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#115929253-C-A

75791661-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 115929263-G-C

75791809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115929413-T-C

75791905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115929505-A-G

75792083-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 115929664-A-G

http://identifiers.org/hco/17/GRCh38#75792084-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#115929665-C-A

75792084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 115929665-C-T

75792096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 115929683-C-T

75792206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 115929776-G-A

75792206-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 115929776-G-T

75792207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 115929777-C-T

75792253-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 115929821-G-T

75792312-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 115929874-G-T

75792392-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115929954-T-C

75792473-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115930180-T-C

http://identifiers.org/hco/17/GRCh38#75792526-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#115930232-C-A

75792531-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 115930237-T-C

75792791-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 115931271-A-G

75792830-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 115931308-T-C

75792897-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 115931355-A-G

75793078-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 115931523-A-T

75793180-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 115931597-A-G

http://identifiers.org/hco/17/GRCh38#75793301-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#115931684-C-A

75793301-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 115931684-C-G

75793301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 115931684-C-T

75793321-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 115931703-A-G

75793361-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 115931736-A-G

http://identifiers.org/hco/17/GRCh38#75793370-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#115931745-C-A

75793370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 115931745-C-T

75793404-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 115931779-A-G

75793404-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 115931779-A-T

75793814-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115932118-T-C

75793885-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115932187-C-G

75793886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115932188-C-T

75793922-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115932223-T-C

75794042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115932337-G-A

http://identifiers.org/hco/17/GRCh38#75794046-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#115932341-A-C

75794083-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115932374-T-A

75794083-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115932374-T-G

75809345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 115938166-A-G

75809385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 115938203-G-A

75809403-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 115938220-A-G

http://identifiers.org/hco/17/GRCh38#75809497-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#115938308-A-C

75809552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 115938352-T-C

75809620-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 115938407-T-C

75809623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 115938410-G-A

75809623-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 115938410-G-T

75809747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 115938490-G-A

75809747-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 115938490-G-T

http://identifiers.org/hco/17/GRCh38#75810020-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#115938758-A-C

75810020-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 115938758-A-G

75810032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 115938770-G-A

75810032-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 115938770-G-C

75810032-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 115938770-G-T

75810081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 115938816-C-T

http://identifiers.org/hco/17/GRCh38#75812079-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#115939778-C-A

75812250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 115939949-C-T

75812374-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 115940052-A-G

75812435-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 115940115-G-C

75812441-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 115940126-T-C

75812445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 115940130-C-T

http://identifiers.org/hco/17/GRCh38#75812626-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#115940304-C-A

75812626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 115940304-C-T

75812629-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 115940307-C-T

75812635-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 115940313-G-T

75812645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 115940322-G-A

75812645-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 115940322-G-T

75812678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 115940352-A-G

http://identifiers.org/hco/17/GRCh38#75812687-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#115940363-C-A

75812687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 115940363-C-T

75812697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 115940373-C-T

http://identifiers.org/hco/17/GRCh38#75812726-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#115940407-A-C

75812726-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 115940407-A-G

75812870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 115940619-G-A

http://identifiers.org/hco/17/GRCh38#75812948-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#115940729-C-A

75812948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 115940729-C-T

http://identifiers.org/hco/17/GRCh38#75812953-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#115940734-C-A

75812953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 115940734-C-T

http://identifiers.org/hco/17/GRCh38#75813005-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#115940788-C-A

75813005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 115940788-C-T

75813037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 115940823-G-A

75813037-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 115940823-G-T

http://identifiers.org/hco/17/GRCh38#75813038-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#115940824-C-A

75813038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 115940824-C-T

75813064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 115940849-G-A

75813064-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 115940849-G-T

75813343-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 115941123-G-T

75813357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 115941137-G-A

75813357-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 115941137-G-T

75813373-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 115941153-T-G

http://identifiers.org/hco/17/GRCh38#75813622-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#115941368-C-A

75813622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 115941368-C-T

75813739-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 115941493-A-T

75813764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 115941516-G-A

75813764-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 115941516-G-C

75813764-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 115941516-G-T

http://identifiers.org/hco/17/GRCh38#75815092-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#115942097-C-A

75815096-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 115942101-T-C

75815096-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 115942101-T-G

75815129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 115942237-T-C

75815129-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 115942237-T-G

75815164-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant, undefined
orthologous variants: 115942277-T-C

http://identifiers.org/hco/17/GRCh38#75815378-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#115942445-A-C

75816076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: intron variant
orthologous variants: 115943247-C-T

75816141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: intron variant
orthologous variants: 115943311-C-T

75816370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: intron variant
orthologous variants: 115943517-G-A

http://identifiers.org/hco/17/GRCh38#75816663-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#115943752-C-A

75816663-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: intron variant
orthologous variants: 115943752-C-G

75816663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: intron variant
orthologous variants: 115943752-C-T

75816664-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: intron variant
orthologous variants: 115943753-T-G

75816679-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: intron variant
orthologous variants: 115943767-A-G

75816718-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: intron variant
orthologous variants: 115943791-G-T

75816727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: intron variant
orthologous variants: 115943800-G-A

75816727-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: intron variant
orthologous variants: 115943800-G-T

75816752-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: intron variant
orthologous variants: 115943827-T-C

http://identifiers.org/hco/17/GRCh38#75816754-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#115943829-C-A

75816754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: intron variant
orthologous variants: 115943829-C-T

75816835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: missense variant
orthologous variants: 115943907-G-A

75816835-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: missense variant
orthologous variants: 115943907-G-T

http://identifiers.org/hco/17/GRCh38#75816912-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#115943984-C-A

75816912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 115943984-C-T

75816985-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: intron variant
orthologous variants: 115944053-A-G

75817081-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: intron variant
orthologous variants: 115944104-G-T

75817267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: intron variant
orthologous variants: 115944259-G-A

75817267-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: intron variant
orthologous variants: 115944259-G-T

75817276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: intron variant
orthologous variants: 115944268-C-T

75817658-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: intron variant
orthologous variants: 115944660-A-G

75817692-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: intron variant
orthologous variants: 115944681-G-C

75817952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: intron variant
orthologous variants: 115945038-G-A

75817952-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: intron variant
orthologous variants: 115945038-G-T

75817954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: intron variant
orthologous variants: 115945040-G-A

75817954-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: intron variant
orthologous variants: 115945040-G-T

75818261-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: intron variant
orthologous variants: 115945376-T-C

75818505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: intron variant
orthologous variants: 115945558-G-A

75818505-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: intron variant
orthologous variants: 115945558-G-T

http://identifiers.org/hco/17/GRCh38#75818734-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#115945755-A-C

75818745-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: missense variant
orthologous variants: 115945766-G-T

75818978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115946032-T-C

75818988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115946047-G-A

75818991-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115946050-T-A

http://identifiers.org/hco/17/GRCh38#75819018-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#115946099-C-A

75819018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115946099-C-T

75819110-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115946204-G-T

75819447-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115946473-G-T

75819477-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115946503-G-T

75819615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115946667-G-A

75819615-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115946667-G-T

75819774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 115946897-G-A

75819784-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 115946907-C-G

75819784-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 115946907-C-T

75819796-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115946919-T-C

75819796-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115946919-T-G

http://identifiers.org/hco/17/GRCh38#75819893-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#115946992-C-A

75819893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115946992-C-T

http://identifiers.org/hco/17/GRCh38#75819895-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#115946994-C-A

75819895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115946994-C-T

75819960-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 115947057-C-G

75819960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 115947057-C-T

75820011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 115947108-C-T

75820074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: synonymous variant
orthologous variants: 115947171-A-G

75820152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: intron variant
orthologous variants: 115947231-C-T

75820171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: intron variant
orthologous variants: 115947250-C-T

75820181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: intron variant
orthologous variants: 115947260-C-T

http://identifiers.org/hco/17/GRCh38#75820182-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#115947261-C-A

75820182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: intron variant
orthologous variants: 115947261-C-T

75820193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: intron variant
orthologous variants: 115947272-A-G

75820206-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: intron variant
orthologous variants: 115947284-T-G

75820249-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: intron variant
orthologous variants: 115947326-T-C

75820385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: intron variant
orthologous variants: 115947444-C-T

75820454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: intron variant
orthologous variants: 115947507-G-A

75820572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: intron variant
orthologous variants: 115947684-C-T

75820602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: intron variant
orthologous variants: 115947712-G-A

75821285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: intron variant
orthologous variants: 115948157-G-A

75821297-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: intron variant
orthologous variants: 115948169-T-C

75821298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: intron variant
orthologous variants: 115948170-G-A

75821691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: intron variant
orthologous variants: 115948484-G-A

75821747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: intron variant
orthologous variants: 115948537-G-A

75821830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: intron variant
orthologous variants: 115948580-G-A

75821928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: intron variant
orthologous variants: 115948639-G-A

75821928-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: intron variant
orthologous variants: 115948639-G-C

75821928-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: intron variant
orthologous variants: 115948639-G-T

http://identifiers.org/hco/17/GRCh38#75821967-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#115948675-C-A

75822011-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: intron variant
orthologous variants: 115948717-T-C

75822400-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: intron variant
orthologous variants: 115948999-G-C

75822400-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: intron variant
orthologous variants: 115948999-G-T

75822849-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: intron variant
orthologous variants: 115949429-T-C

75823161-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: intron variant
orthologous variants: 115949706-T-A

75823161-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: intron variant
orthologous variants: 115949706-T-C

75823179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: intron variant
orthologous variants: 115949724-G-A

http://identifiers.org/hco/17/GRCh38#75823190-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#115949735-C-A

http://identifiers.org/hco/17/GRCh38#75823195-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#115949740-A-C

75823260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 115949810-C-T

75823315-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: synonymous variant
orthologous variants: 115949865-T-C

75823411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: synonymous variant
orthologous variants: 115949961-G-A

75823411-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: synonymous variant
orthologous variants: 115949961-G-T

75823456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: synonymous variant
orthologous variants: 115950006-G-A

75823456-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: synonymous variant
orthologous variants: 115950006-G-T

http://identifiers.org/hco/17/GRCh38#75823468-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#115950018-C-A

75823468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: synonymous variant
orthologous variants: 115950018-C-T

http://identifiers.org/hco/17/GRCh38#75823530-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#115950080-C-A

75823530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 115950080-C-T

75823532-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: intron variant
orthologous variants: 115950082-G-C

75823532-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: intron variant
orthologous variants: 115950082-G-T

75823559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: intron variant
orthologous variants: 115950112-G-A

75823559-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: intron variant
orthologous variants: 115950112-G-C

75823559-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: intron variant
orthologous variants: 115950112-G-T

75823641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: intron variant
orthologous variants: 115950132-A-G

75823665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: intron variant
orthologous variants: 115950153-G-A

75823665-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: intron variant
orthologous variants: 115950153-G-T

75824109-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: intron variant
orthologous variants: 115950494-C-G

http://identifiers.org/hco/17/GRCh38#75824113-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#115950498-C-A

75824113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: intron variant
orthologous variants: 115950498-C-T

http://identifiers.org/hco/17/GRCh38#75824120-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#115950505-C-A

75824182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: intron variant
orthologous variants: 115950560-G-A

75824182-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: intron variant
orthologous variants: 115950560-G-T

75824215-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: intron variant
orthologous variants: 115950593-T-G

http://identifiers.org/hco/17/GRCh38#75824242-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#115950629-C-A

75824242-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: intron variant
orthologous variants: 115950629-C-G

75824242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: intron variant
orthologous variants: 115950629-C-T

http://identifiers.org/hco/17/GRCh38#75824378-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#115950765-C-A

75824378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: synonymous variant
orthologous variants: 115950765-C-T

75824429-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: 3 prime UTR variant
orthologous variants: 115950816-T-A

75824429-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: 3 prime UTR variant
orthologous variants: 115950816-T-C

75824597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: 3 prime UTR variant
orthologous variants: 115950946-C-T

75824986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: 3 prime UTR variant
orthologous variants: 115951287-G-A

75824986-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: 3 prime UTR variant
orthologous variants: 115951287-G-T

75825175-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: 3 prime UTR variant
orthologous variants: 115951451-G-T

http://identifiers.org/hco/17/GRCh38#75825254-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#115951522-C-A

75825254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: 3 prime UTR variant
orthologous variants: 115951522-C-T

75825314-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: 3 prime UTR variant
orthologous variants: 115951584-T-C

http://identifiers.org/hco/17/GRCh38#75825433-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#115951697-C-A

75825433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: 3 prime UTR variant
orthologous variants: 115951697-C-T

75825473-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: 3 prime UTR variant
orthologous variants: 115951735-T-C

75825658-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: 3 prime UTR variant
orthologous variants: 115951907-G-A

75825660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: 3 prime UTR variant
orthologous variants: 115951909-G-A

http://identifiers.org/hco/17/GRCh38#75825672-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#115951921-C-A

75825799-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29369
most severe consequence: 3 prime UTR variant
orthologous variants: 115952041-A-G