76471036-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 116489158-T-C

http://identifiers.org/hco/17/GRCh38#76471121-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116489368-C-A

http://identifiers.org/hco/17/GRCh38#76471142-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116489391-C-A

76471145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 116489394-T-C

http://identifiers.org/hco/17/GRCh38#76471229-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116489513-C-A

76471229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 116489513-C-T

76471238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 116489522-C-T

http://identifiers.org/hco/17/GRCh38#76471244-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116489528-C-A

76471244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 116489528-C-T

http://identifiers.org/hco/17/GRCh38#76471282-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116489566-A-C

76471282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 116489566-A-G

76471388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 116489653-G-A

76471390-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 116489655-T-G

76471428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 116489694-G-A

76471428-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 116489694-G-T

http://identifiers.org/hco/17/GRCh38#76471435-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116489715-C-A

76471435-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 116489715-C-G

76471435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 116489715-C-T

http://identifiers.org/hco/17/GRCh38#76471469-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116489748-C-A

76471469-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 116489748-C-G

76471490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 116489769-G-A

76471490-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 116489769-G-C

76471490-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 116489769-G-T

76471544-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 116489807-C-G

76471544-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 116489807-C-T

76471568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 116489820-G-A

76471568-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 116489820-G-T

76471569-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 116489821-A-G

76471570-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 116489822-G-T

http://identifiers.org/hco/17/GRCh38#76471639-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116489851-C-A

76471639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116489851-C-T

76471680-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116489892-T-G

76471768-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116489980-A-G

76471969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116490181-G-A

76471969-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116490181-G-C

76471969-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116490181-G-T

76471980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116490192-G-A

76471980-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116490192-G-C

76471980-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116490192-G-T

76472035-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116490247-T-A

76472035-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116490247-T-C

76472166-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 116490339-T-A

76472166-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 116490339-T-C

http://identifiers.org/hco/17/GRCh38#76472216-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116490365-C-A

76472316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116490444-G-A

76472316-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116490444-G-T

http://identifiers.org/hco/17/GRCh38#76472494-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116490564-C-A

76472494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116490564-C-T

http://identifiers.org/hco/17/GRCh38#76472582-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116490652-C-A

76472582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116490652-C-T

76472612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116490680-C-T

76472698-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116490899-T-C

76472701-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116490902-G-C

76472867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116491088-C-T

76472944-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116491166-A-G

76473021-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116491240-G-C

http://identifiers.org/hco/17/GRCh38#76473324-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116491508-A-C

76473324-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116491508-A-G

76473400-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116491570-G-T

http://identifiers.org/hco/17/GRCh38#76473401-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116491571-C-A

76473401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116491571-C-T

76473405-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116491575-T-A

76473405-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116491575-T-C

76473420-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116491581-T-C

76473420-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116491581-T-G

76473529-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116491673-T-G

http://identifiers.org/hco/17/GRCh38#76473641-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#116491714-C-A

76473641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 116491714-C-T

76473725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116491798-G-A

76473754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116491827-G-A

76473754-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116491827-G-T

76473914-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116491987-G-T

76473919-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116491992-G-A

76473963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116492047-G-A

76473963-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116492047-G-T

76474100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116492175-G-A

76474100-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116492175-G-T

76474103-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116492178-C-G

76474157-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116492230-A-G

http://identifiers.org/hco/17/GRCh38#76474161-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116492234-C-A

76474161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116492234-C-T

76474177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116492248-G-A

76474177-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116492248-G-T

76474182-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116492253-A-G

http://identifiers.org/hco/17/GRCh38#76474226-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116492298-C-A

76474226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116492298-C-T

http://identifiers.org/hco/17/GRCh38#76474272-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116492360-C-A

76474272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116492360-C-T

76474317-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116492396-T-A

76474317-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116492396-T-C

76474406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116492453-G-A

http://identifiers.org/hco/17/GRCh38#76474466-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116492513-C-A

76474466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116492513-C-T

76474493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116492540-G-A

76474502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116492549-T-C

76474502-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116492549-T-G

76474555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116492598-G-A

76474555-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116492598-G-T

76474582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116492625-T-C

76474721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 116492707-G-A

76474769-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116492754-C-T

76474888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116492879-G-A

76474888-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116492879-G-C

76474929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116492918-G-A

76474929-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116492918-G-C

76474929-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116492918-G-T

76474953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116492942-G-A

76474963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116492952-G-A

76474963-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116492952-G-T

76475145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 116493130-T-C

http://identifiers.org/hco/17/GRCh38#76475155-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116493140-C-A

76475155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116493140-C-T

http://identifiers.org/hco/17/GRCh38#76475188-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116493173-C-A

76475188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116493173-C-T

http://identifiers.org/hco/17/GRCh38#76475209-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116493179-C-A

76475209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116493179-C-T

http://identifiers.org/hco/17/GRCh38#76475523-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116493490-A-C

76475783-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116493665-T-C

http://identifiers.org/hco/17/GRCh38#76475828-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116493678-C-A

76475828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116493678-C-T

http://identifiers.org/hco/17/GRCh38#76476642-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116494281-C-A

76476642-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116494281-C-G

76476661-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116494300-T-C

http://identifiers.org/hco/17/GRCh38#76476665-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116494303-C-A

76476665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116494303-C-T

76476739-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116494377-C-G

76476740-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116494378-T-C

76476771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116494413-G-A

76476771-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116494413-G-T

76476916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116494565-G-A

76476991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116494640-G-A

76476991-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116494640-G-C

76477182-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 116494760-A-G

76477257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116494835-G-A

76477257-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116494835-G-C

76477313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116494891-A-G

http://identifiers.org/hco/17/GRCh38#76477368-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116494945-C-A

76477368-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116494945-C-G

76477378-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116494955-A-T

http://identifiers.org/hco/17/GRCh38#76477420-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116494992-C-A

76477444-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116495010-G-T

76477532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116495086-G-A

76477532-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116495086-G-T

76477594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116495142-G-A

76477594-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116495142-G-T

76477603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116495151-C-T

76477696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116495243-G-A

76477696-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116495243-G-C

76477696-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116495243-G-T

76477723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116495270-G-A

76477806-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116495351-A-G

76477807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116495352-G-A

76477939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116495415-C-T

76478983-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116495964-C-G

76478983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116495964-C-T

76479032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116496019-G-A

76479062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116496049-C-T

76479097-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116496084-G-C

76479112-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116496099-A-T

http://identifiers.org/hco/17/GRCh38#76479291-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116496277-C-A

76479293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116496279-A-G

76479293-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116496279-A-T

76479294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116496280-G-A

76479294-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116496280-G-T

76479309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116496303-A-G

http://identifiers.org/hco/17/GRCh38#76479310-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116496304-C-A

76479310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116496304-C-T

76479390-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116496420-G-T

76479391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116496421-G-A

76479391-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116496421-G-T

http://identifiers.org/hco/17/GRCh38#76479401-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116496442-C-A

76479401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116496442-C-T

http://identifiers.org/hco/17/GRCh38#76479455-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116496500-C-A

76479455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116496500-C-T

76479484-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116496604-C-G

http://identifiers.org/hco/17/GRCh38#76479495-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116496627-A-C

76479495-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116496627-A-T

http://identifiers.org/hco/17/GRCh38#76479526-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116496655-C-A

http://identifiers.org/hco/17/GRCh38#76479538-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116496727-C-A

76479538-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116496727-C-T

76479596-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116496824-A-G

76479596-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116496824-A-T

76479671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116496880-G-A

76479671-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116496880-G-T

76479676-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116496885-C-G

76479676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116496885-C-T

76479677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116496886-G-A

76479677-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116496886-G-T

76479692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116496901-G-A

76479692-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116496901-G-T

76479762-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 116496963-G-T

http://identifiers.org/hco/17/GRCh38#76479927-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116497125-C-A

http://identifiers.org/hco/17/GRCh38#76481182-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#116497917-C-A

76481182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116497917-C-T

76481220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116497955-G-A

http://identifiers.org/hco/17/GRCh38#76481253-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116497969-C-A

76481253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116497969-C-T

76481323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116498016-G-A

76481323-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116498016-G-T

http://identifiers.org/hco/17/GRCh38#76481368-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116498048-C-A

http://identifiers.org/hco/17/GRCh38#76481402-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116498081-A-C

76481468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 116498141-C-T

http://identifiers.org/hco/17/GRCh38#76481494-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116498167-C-A

76481494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116498167-C-T

http://identifiers.org/hco/17/GRCh38#76481546-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116498223-C-A

76481546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 116498223-C-T

76481554-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116498231-G-T

http://identifiers.org/hco/17/GRCh38#76481570-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116498245-C-A

76481570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116498245-C-T

76481571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116498246-G-A

76481571-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116498246-G-T

76481648-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116498320-A-G

76481648-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116498320-A-T

76481669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116498343-G-A

76481669-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116498343-G-T

http://identifiers.org/hco/17/GRCh38#76481719-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#116498371-C-A

76481719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116498371-C-T

76481724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116498376-G-A

76481724-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116498376-G-T

76481725-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116498377-T-C

76481730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116498382-G-A

76481730-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116498382-G-C

76481730-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116498382-G-T

76482202-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116498558-T-C

76482217-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116498573-G-T

76482512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116498899-G-A

http://identifiers.org/hco/17/GRCh38#76482521-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116498908-C-A

76482521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116498908-C-T

http://identifiers.org/hco/17/GRCh38#76482770-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#116499101-C-A

76486634-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116500814-A-T

76486856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116500988-C-T

76486880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116501007-C-T

76486918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116501052-C-T

76489700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116503332-C-T

http://identifiers.org/hco/17/GRCh38#76489859-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116503475-C-A

76490143-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116503776-T-C

76490143-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116503776-T-G

76490194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116503813-G-A

76490446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116503990-C-T

76490601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116504127-G-A

76490601-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116504127-G-C

76490603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116504129-T-C

76490955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116505783-C-T

76491301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116506048-G-A

76491332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116506094-C-T

76491544-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116506269-C-T

76491563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116506289-G-A

76491585-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116506308-C-G

76491664-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116506388-C-G

76491747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116506462-G-A

76491747-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116506462-G-T

76491754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116506469-C-T

http://identifiers.org/hco/17/GRCh38#76491784-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116506496-C-A

76491784-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116506496-C-T

76491860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116506593-G-A

76492019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116506750-C-T

76492094-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116506845-A-G

76492270-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116507006-T-C

http://identifiers.org/hco/17/GRCh38#76492280-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116507016-C-A

76492450-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116507204-C-G

76492663-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116507382-T-A

76492666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116507385-C-T

76492724-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116507422-C-G

76492735-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116507432-C-G

76492807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116507494-G-A

76493030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116507695-G-A

76493030-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116507695-G-T

76493123-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116507757-G-A

76493123-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116507757-G-T

76493127-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116507761-T-C

76493219-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116507852-T-G

76493319-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116508021-G-C

76493354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116508057-G-A

76493356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116508060-C-T

76493462-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116508162-A-G

76493727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116508368-C-T

76493729-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116508370-G-C

76494654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116509244-A-G

76494696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116509278-G-A

http://identifiers.org/hco/17/GRCh38#76494756-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116509336-A-C

76494789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116509354-G-A

76495052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116509483-G-A

76495141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116509560-C-T

76495548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116509941-G-A

76496001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116510395-C-T

76496311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116510617-T-C

76496381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116510681-G-A

76497109-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116511298-T-C

76497113-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116511302-A-T

76497524-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116511526-C-G

76497524-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116511526-C-T

76497525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116511527-G-A

76497610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116511584-C-T

76497747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116511714-G-A

76497925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116511857-C-T

76497949-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116511881-T-A

http://identifiers.org/hco/17/GRCh38#76498572-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#116512465-A-C

76498761-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116512795-G-T

76498767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116512801-C-T

76498839-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116512877-T-A

76498839-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116512877-T-G

76498841-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116512879-T-C

76499118-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116513132-C-G

http://identifiers.org/hco/17/GRCh38#76499232-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116513235-C-A

76499615-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116513539-C-G

76499615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116513539-C-T

76499755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116513677-C-T

76499956-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116513847-A-G

76500018-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116513868-G-C

76500019-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116513869-T-A

76500522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116514255-C-T

76500556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116514271-C-T

http://identifiers.org/hco/17/GRCh38#76500662-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116514375-C-A

http://identifiers.org/hco/17/GRCh38#76500786-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116514471-C-A

76500786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116514471-C-T

http://identifiers.org/hco/17/GRCh38#76500829-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116514514-C-A

76500831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116514516-C-T

76500909-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116514601-T-C

76500938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 116514630-G-A

76500938-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 116514630-G-T

76501052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116514752-G-A

76501052-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116514752-G-T

76501103-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116514805-T-A

76501103-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116514805-T-C

76501124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 116514825-G-A

76501124-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 116514825-G-C

76501124-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 116514825-G-T

http://identifiers.org/hco/17/GRCh38#76501143-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116514844-C-A

76501143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116514844-C-T

76501180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 116514878-C-T

http://identifiers.org/hco/17/GRCh38#76501210-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#116514888-C-A

76501210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 116514888-C-T

76501220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116514898-G-A

76501220-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116514898-G-T

76501244-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 116514918-T-C

http://identifiers.org/hco/17/GRCh38#76501286-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#116514937-C-A

76501286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 116514937-C-T

76501297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 116514948-C-T

http://identifiers.org/hco/17/GRCh38#76501306-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116514957-C-A

76501306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116514957-C-T

http://identifiers.org/hco/17/GRCh38#76501346-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#116514997-C-A

76501346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 116514997-C-T

76501382-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 116515032-A-G

76501405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 116515054-G-A

76501405-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 116515054-G-C

76501405-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 116515054-G-T

76501443-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: intron variant
orthologous variants: 116515089-T-C

76501465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 116515111-G-A

76501465-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 116515111-G-T

76501495-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 116515135-A-G

76501503-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 116515143-T-C

76501503-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 116515143-T-G

76501514-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: 5 prime UTR variant
orthologous variants: 116515150-A-G

http://identifiers.org/hco/17/GRCh38#76501609-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116515206-C-A

76501609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: 5 prime UTR variant
orthologous variants: 116515206-C-T

76501645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 116515233-C-T

http://identifiers.org/hco/17/GRCh38#76501762-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#116515368-C-A

76501762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 116515368-C-T

76501772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20788
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 116515378-C-T