1107682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: 3 prime UTR variant
orthologous variants: 79892873-G-A

1107682-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: 3 prime UTR variant
orthologous variants: 79892873-G-T

1107690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: 3 prime UTR variant
orthologous variants: 79892879-G-A

1107690-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: 3 prime UTR variant
orthologous variants: 79892879-G-T

1107733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: 3 prime UTR variant
orthologous variants: 79892915-A-G

http://identifiers.org/hco/19/GRCh38#1107743-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#79892927-C-A

1107743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: 3 prime UTR variant
orthologous variants: 79892927-C-T

http://identifiers.org/hco/19/GRCh38#1107765-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#79892951-C-A

1107765-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: 3 prime UTR variant
orthologous variants: 79892951-C-G

1107765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: 3 prime UTR variant
orthologous variants: 79892951-C-T

http://identifiers.org/hco/19/GRCh38#1107789-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#79892974-A-C

1107789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: 3 prime UTR variant
orthologous variants: 79892974-A-G

1107964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: 3 prime UTR variant
orthologous variants: 79893092-G-A

1107964-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: 3 prime UTR variant
orthologous variants: 79893092-G-T

1107997-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: 3 prime UTR variant
orthologous variants: 79893106-A-G

1107997-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: 3 prime UTR variant
orthologous variants: 79893106-A-T

1108169-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: 3 prime UTR variant
orthologous variants: 79893189-T-C

1108169-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: 3 prime UTR variant
orthologous variants: 79893189-T-G

1108193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: 3 prime UTR variant
orthologous variants: 79893214-T-C

1108252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 79893270-G-A

http://identifiers.org/hco/19/GRCh38#1108511-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#79893508-C-A

1108511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 79893508-C-T

http://identifiers.org/hco/19/GRCh38#1108577-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#79893574-C-A

1108577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 79893574-C-T

1108678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 79893672-G-A

1108678-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: missense_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 79893672-G-T

1108707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 79893709-G-A

1108707-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 79893709-G-T

1108709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 79893711-G-A

1108709-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 79893711-G-T

1108714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79893716-G-A

1108714-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79893716-G-C

1108714-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79893716-G-T

1108716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79893718-G-A

1108716-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79893718-G-T

1108717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79893719-C-T

http://identifiers.org/hco/19/GRCh38#1108726-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#79893728-C-A

1108726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79893728-C-T

http://identifiers.org/hco/19/GRCh38#1108885-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#79893896-C-A

1108885-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 79893896-C-G

1108885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 79893896-C-T

http://identifiers.org/hco/19/GRCh38#1108915-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#79893926-C-A

1108915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 79893926-C-T

1109187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 79894139-G-A

1109187-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 79894139-G-T

1109192-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 79894144-T-A

1109192-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 79894144-T-C

http://identifiers.org/hco/19/GRCh38#1109252-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#79894202-C-A

1109252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79894202-C-T

1109259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79894215-C-T

1109316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 79894274-G-A

1109316-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 79894274-G-C

1109316-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 79894274-G-T

http://identifiers.org/hco/19/GRCh38#1109340-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#79894298-C-A

1109340-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 79894298-C-G

1109340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 79894298-C-T

http://identifiers.org/hco/19/GRCh38#1109409-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#79894367-C-A

1109409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 79894367-C-T

1109489-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79894445-A-T

http://identifiers.org/hco/19/GRCh38#1109490-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#79894446-C-A

1109490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79894446-C-T

1109584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 79894549-G-A

1109584-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 79894549-G-T

1109665-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79894621-G-C

1109785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 79894741-G-A

1109785-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 79894741-G-T

1109798-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79894754-T-A

1109798-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79894754-T-C

1109803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79894759-G-A

1109803-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79894759-G-C

1109803-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79894759-G-T

http://identifiers.org/hco/19/GRCh38#1111032-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#79896012-C-A

1111041-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 79896021-A-G

1111100-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 79896080-G-T

1111324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79896141-C-T

http://identifiers.org/hco/19/GRCh38#1111466-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#79896189-C-A

http://identifiers.org/hco/19/GRCh38#1111474-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#79896197-C-A

1111474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79896197-C-T

http://identifiers.org/hco/19/GRCh38#1111590-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#79896312-C-A

http://identifiers.org/hco/19/GRCh38#1112059-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: missense_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#79896487-C-A

1112116-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron variant
orthologous variants: 79896534-T-C

http://identifiers.org/hco/19/GRCh38#1112261-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, stop_gained
orthologous variants: http://identifiers.org/mco/10/GRCm39#79896695-A-C

1112261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 79896695-A-G

1112267-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 79896701-T-A

1112267-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 79896701-T-C

1112267-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 79896701-T-G

1112374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron variant
orthologous variants: 79896791-G-A

1112374-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron variant
orthologous variants: 79896791-G-C

1112374-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron variant
orthologous variants: 79896791-G-T

1112627-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron variant
orthologous variants: 79897016-G-C

1112627-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron variant
orthologous variants: 79897016-G-T

1112698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, undefined
orthologous variants: 79897065-G-A

1112698-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, undefined
orthologous variants: 79897065-G-T

http://identifiers.org/hco/19/GRCh38#1112811-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, splice_region_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#79897144-C-A

1112811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, splice_region_variant, undefined
orthologous variants: 79897144-C-T

http://identifiers.org/hco/19/GRCh38#1112815-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#79897147-C-A

1112815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron variant
orthologous variants: 79897147-C-T

1112866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: synonymous_variant, undefined
orthologous variants: 79897198-G-A

1112866-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: synonymous_variant, undefined
orthologous variants: 79897198-G-T

1112988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, undefined
orthologous variants: 79897328-G-A

1112988-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, undefined
orthologous variants: 79897328-G-T

http://identifiers.org/hco/19/GRCh38#1112997-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#79897337-C-A

1112997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, undefined
orthologous variants: 79897337-C-T

1113234-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron variant
orthologous variants: 79897611-T-A

1113577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: synonymous_variant, undefined
orthologous variants: 79898038-G-A

1113589-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: synonymous_variant, undefined
orthologous variants: 79898050-G-A

1113589-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: synonymous_variant, undefined
orthologous variants: 79898050-G-C

1113598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: synonymous_variant, undefined
orthologous variants: 79898059-T-C

1113716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, undefined
orthologous variants: 79898177-G-A

1113721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, undefined
orthologous variants: 79898182-G-A

1113721-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, undefined
orthologous variants: 79898182-G-T

1114248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: missense variant
orthologous variants: 79898419-A-G

1114447-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron variant
orthologous variants: 79898610-A-G

http://identifiers.org/hco/19/GRCh38#1114457-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#79898620-C-A

1114457-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron variant
orthologous variants: 79898620-C-G

1114457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron variant
orthologous variants: 79898620-C-T

1114465-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron variant
orthologous variants: 79898626-G-T

1114482-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron variant
orthologous variants: 79898650-A-G

1115977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79899443-G-A

1115977-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79899443-G-C

1115977-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79899443-G-T

http://identifiers.org/hco/19/GRCh38#1115979-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#79899445-A-C

1115979-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79899445-A-G

1115979-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79899445-A-T

1116100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 79899559-G-A

1116100-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 79899559-G-C

1116100-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 79899559-G-T

1116187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79899641-G-A

1116187-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79899641-G-C

1116187-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79899641-G-T

1116230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79899683-G-A

1116230-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79899683-G-T

1116239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79899689-G-A

1116239-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79899689-G-T

http://identifiers.org/hco/19/GRCh38#1116789-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#79899931-C-A

1116789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79899931-C-T

http://identifiers.org/hco/19/GRCh38#1116799-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#79899947-C-A

1116799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79899947-C-T

http://identifiers.org/hco/19/GRCh38#1116802-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#79899953-C-A

1116802-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79899953-C-G

1116802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79899953-C-T

http://identifiers.org/hco/19/GRCh38#1116816-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#79899966-C-A

1116816-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79899966-C-G

1116816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79899966-C-T

1116837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 79899987-C-T

1118231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79901656-G-A

1118327-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79901733-G-T

1118391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79901811-G-A

http://identifiers.org/hco/19/GRCh38#1118812-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#79902170-C-A

1118932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79902285-G-A

1118932-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79902285-G-T

http://identifiers.org/hco/19/GRCh38#1119024-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#79902397-C-A

1119024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 79902397-C-T

1119050-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 79902423-G-T

1119101-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 79902474-G-C

1119137-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 79902510-G-T

1119161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 79902534-G-A

1119161-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 79902534-G-C

1119161-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 79902534-G-T

1119240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79902567-C-T

1119391-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79902599-A-G

http://identifiers.org/hco/19/GRCh38#1119487-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#79902636-C-A

1119487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79902636-C-T

1119496-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79902645-T-A

1119496-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79902645-T-C

1119496-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79902645-T-G

1119667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79902830-G-A

1119669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79902832-G-A

1119669-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79902832-G-T

1119695-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79902853-G-C

1119695-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79902853-G-T

1119708-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79902879-A-G

1119708-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79902879-A-T

1119711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79902882-G-A

1119711-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79902882-G-C

http://identifiers.org/hco/19/GRCh38#1119736-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#79902905-C-A

1119736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79902905-C-T

1119739-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79902908-G-T

1119913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 79903118-G-A

1119913-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 79903118-G-T

1119947-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 79903152-T-C

http://identifiers.org/hco/19/GRCh38#1119964-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#79903169-A-C

1119964-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 79903169-A-G

1119964-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 79903169-A-T

1119991-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 79903196-A-G

1120012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 79903217-G-A

1120012-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 79903217-G-T

http://identifiers.org/hco/19/GRCh38#1122128-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#79904151-C-A

1122128-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79904151-C-G

1122128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79904151-C-T

1122406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79904430-G-A

1122419-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79904444-A-G

1122419-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79904444-A-T

http://identifiers.org/hco/19/GRCh38#1122562-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#79904613-C-A

1122562-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 79904613-C-G

1122562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 79904613-C-T

http://identifiers.org/hco/19/GRCh38#1122582-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#79904634-C-A

1122582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79904634-C-T

http://identifiers.org/hco/19/GRCh38#1122624-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#79904666-C-A

1122624-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79904666-C-G

1122624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79904666-C-T

1122804-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79904938-A-G

1122830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79905011-G-A

1122830-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79905011-G-T

1122872-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79905090-T-C

1122873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79905091-G-A

1122873-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79905091-G-T

http://identifiers.org/hco/19/GRCh38#1122887-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#79905105-C-A

1122887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 79905105-C-T

http://identifiers.org/hco/19/GRCh38#1122941-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#79905163-C-A

1122941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 79905163-C-T

1122957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 79905182-G-A

1122957-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 79905182-G-T

1123361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79905352-G-A

1123607-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 79905518-C-G

1123607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 79905518-C-T

1123657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79905561-G-A

1123657-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79905561-G-T

1123797-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79905674-G-T

1123800-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79905677-T-A

1123800-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79905677-T-C

1123821-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79905698-T-C

http://identifiers.org/hco/19/GRCh38#1123825-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#79905702-C-A

1123825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79905702-C-T

http://identifiers.org/hco/19/GRCh38#1126287-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#79907124-C-A

1126287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79907124-C-T

1127616-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 79908203-G-C

1127616-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 79908203-G-T

http://identifiers.org/hco/19/GRCh38#1127718-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#79908305-C-A

1127718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 79908305-C-T

1127757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 79908344-G-A

1127757-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 79908344-G-C

1131965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79910994-G-A

1131965-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79910994-G-C

1131965-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79910994-G-T

1132002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79911032-G-A

1132002-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79911032-G-C

1132002-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79911032-G-T

1132181-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 79911163-G-A

1132181-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 79911163-G-C

1132181-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 79911163-G-T

1132202-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 79911184-G-A

1132202-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 79911184-G-T

1132373-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, undefined
orthologous variants: 79911347-C-G

1132373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, undefined
orthologous variants: 79911347-C-T

1132377-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, undefined
orthologous variants: 79911351-G-T

1132569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, undefined
orthologous variants: 79911536-G-A

1133106-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron variant
orthologous variants: 79911723-G-C

1140340-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron variant
orthologous variants: 79915772-C-G

1140514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron variant
orthologous variants: 79915949-G-A

1142424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron variant
orthologous variants: 79916456-C-T

http://identifiers.org/hco/19/GRCh38#1147277-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#79918418-C-A

1147277-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron variant
orthologous variants: 79918418-C-G

1147277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron variant
orthologous variants: 79918418-C-T

1149400-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: missense variant
orthologous variants: 79920106-G-A

1149400-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: missense variant
orthologous variants: 79920106-G-T

1154157-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron variant
orthologous variants: 79922063-T-C

1154157-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron variant
orthologous variants: 79922063-T-G

1154324-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: 5 prime UTR variant
orthologous variants: 79922190-A-G

1154330-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: 5 prime UTR variant
orthologous variants: 79922196-G-T

1154338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: 5 prime UTR variant
orthologous variants: 79922204-G-A

1154338-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: 5 prime UTR variant
orthologous variants: 79922204-G-C

1154338-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: 5 prime UTR variant
orthologous variants: 79922204-G-T

1154350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: 5 prime UTR variant
orthologous variants: 79922211-G-A

1154350-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: 5 prime UTR variant
orthologous variants: 79922211-G-C

1154350-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: 5 prime UTR variant
orthologous variants: 79922211-G-T

1154395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: 5 prime UTR variant
orthologous variants: 79922259-A-G

1154395-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: 5 prime UTR variant
orthologous variants: 79922259-A-T

1154414-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron variant
orthologous variants: 79922278-G-T

1154478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron variant
orthologous variants: 79922321-G-A

1154478-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron variant
orthologous variants: 79922321-G-T

http://identifiers.org/hco/19/GRCh38#1154917-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#79922527-A-C

http://identifiers.org/hco/19/GRCh38#1155053-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#79922662-C-A

1155053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron variant
orthologous variants: 79922662-C-T

1155121-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 79922732-G-T

1155189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron variant
orthologous variants: 79922792-G-A

1155189-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron variant
orthologous variants: 79922792-G-T

http://identifiers.org/hco/19/GRCh38#1155201-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#79922802-C-A

1155201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron variant
orthologous variants: 79922802-C-T

http://identifiers.org/hco/19/GRCh38#1163449-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#79931404-C-A

http://identifiers.org/hco/19/GRCh38#1172846-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#79936951-C-A

1172846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79936951-C-T

1172992-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79937087-T-A

1172992-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79937087-T-C

1173501-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79937645-A-G

1173629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 79937834-G-A

1173629-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 79937834-G-T

http://identifiers.org/hco/19/GRCh38#1173758-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#79937972-C-A

1173758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79937972-C-T

http://identifiers.org/hco/19/GRCh38#1173782-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#79937986-C-A

1173885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 79938103-G-A

1173888-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79938106-G-T

http://identifiers.org/hco/19/GRCh38#1174037-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#79938309-C-A

1174037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79938309-C-T

1174067-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79938335-A-G

1174068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79938336-G-A

1174068-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79938336-G-T

1174098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79938367-C-T

1174238-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29158
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79938502-C-G