39009876-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: 3 prime UTR variant
orthologous variants: 53389442-G-T

39009963-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: 3 prime UTR variant
orthologous variants: 53389380-T-C

39009978-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: 3 prime UTR variant
orthologous variants: 53389364-G-T

39009993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: 3 prime UTR variant
orthologous variants: 53389337-G-A

http://identifiers.org/hco/13/GRCh38#39010486-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53388882-C-A

http://identifiers.org/hco/13/GRCh38#39010619-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53388761-C-A

39010619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 53388761-C-T

http://identifiers.org/hco/13/GRCh38#39010874-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53388526-C-A

39010874-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 53388526-C-T

39010985-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 53388424-G-T

39010986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 53388423-G-A

39010986-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 53388423-G-T

39011110-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 53388304-T-A

39011110-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 53388304-T-C

39011112-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 53388302-T-A

39011112-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 53388302-T-C

39011137-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 53388275-A-G

39011171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 53388241-T-C

39011204-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 53388210-T-C

39011204-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 53388210-T-G

39011372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 53388046-C-T

39011520-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53387901-G-C

39011532-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53387890-T-C

39011540-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53387879-T-A

39011574-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53387850-T-G

39011580-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53387844-T-C

39011985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53387189-G-A

39011985-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53387189-G-T

39012008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53387167-G-A

39012008-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53387167-G-T

39012111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53387101-G-A

39012111-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53387101-G-C

39012162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53387050-C-T

39012269-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53386941-A-G

39012420-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53386818-A-G

39012715-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 53386561-T-C

39012763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53386513-G-A

39012763-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53386513-G-C

39012846-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 53386433-A-T

http://identifiers.org/hco/13/GRCh38#39012910-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#53386369-A-C

39012910-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 53386369-A-T

39013120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 53386183-C-T

39013147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 53386156-G-A

39013267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 53386051-C-T

39013342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 53385976-C-T

39013496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 53385834-G-A

39013496-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 53385834-G-T

39013575-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 53385764-A-G

39013596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 53385743-G-A

39013596-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 53385743-G-T

39013752-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 53385587-T-C

39014098-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 53385256-G-A

39014257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 53385100-G-A

39014257-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 53385100-G-C

39014452-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53384926-A-G

39014461-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53384917-G-C

39014461-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53384917-G-T

39014550-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53384835-A-T

39014588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53384783-T-C

39014588-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53384783-T-G

39016334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53384134-G-A

39016537-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53383953-A-G

39016603-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53383859-A-G

http://identifiers.org/hco/13/GRCh38#39016645-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53383794-A-C

39016741-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53383713-T-G

39016870-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53383600-G-T

39017062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53383435-G-A

39017062-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53383435-G-C

39017307-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53383253-A-G

http://identifiers.org/hco/13/GRCh38#39017310-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53383250-A-C

39017310-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53383250-A-G

39017433-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53383187-T-C

39017436-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53383184-T-C

http://identifiers.org/hco/13/GRCh38#39017437-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53383183-C-A

39017442-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53383178-A-T

39017453-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53383166-A-G

39017487-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53383133-A-G

39017559-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53383061-A-G

39017590-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53383035-T-C

http://identifiers.org/hco/13/GRCh38#39017602-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53383023-A-C

http://identifiers.org/hco/13/GRCh38#39017607-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53383015-C-A

39017658-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53382960-G-T

39017673-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53382945-T-C

39017681-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53382937-T-G

39022349-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53382806-T-C

39022406-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53382740-T-A

39022406-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53382740-T-C

39022450-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53382694-G-T

39022481-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53382684-T-C

39022491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53382674-A-G

http://identifiers.org/hco/13/GRCh38#39022493-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53382671-C-A

39022498-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53382666-T-A

39022498-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53382666-T-G

39022588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53382613-A-G

39022664-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53382552-G-T

39022704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53382528-G-A

39022704-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53382528-G-T

http://identifiers.org/hco/13/GRCh38#39022707-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53382525-A-C

39022739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53382497-G-A

39022739-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53382497-G-C

39022739-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53382497-G-T

http://identifiers.org/hco/13/GRCh38#39022744-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53382492-A-C

39022778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53382456-G-A

39022778-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53382456-G-T

http://identifiers.org/hco/13/GRCh38#39022850-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53382371-C-A

39022879-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53382340-T-C

39023207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53382047-T-C

39023207-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53382047-T-G

39023340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53381935-G-A

39023340-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53381935-G-T

http://identifiers.org/hco/13/GRCh38#39023691-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53381602-C-A

39023712-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53381580-T-C

39023744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53381557-A-G

http://identifiers.org/hco/13/GRCh38#39023765-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53381553-C-A

39023765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53381553-C-T

39023862-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53381472-A-G

39023862-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53381472-A-T

39023963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53381432-A-G

39023974-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53381422-G-T

39024020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53381371-G-A

39024020-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53381371-G-T

http://identifiers.org/hco/13/GRCh38#39024161-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53381253-C-A

39024207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53381215-T-C

39024445-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53381018-G-C

39024445-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53381018-G-T

39024446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53381017-G-A

39024446-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53381017-G-T

39024449-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53381014-T-A

39024456-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53381007-T-C

39024573-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53380886-A-G

39024584-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53380878-T-C

39024584-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53380878-T-G

39024588-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53380874-A-T

39024630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53380835-C-T

39024656-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53380813-T-C

http://identifiers.org/hco/13/GRCh38#39024670-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53380802-A-C

http://identifiers.org/hco/13/GRCh38#39024703-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53380769-C-A

39024703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53380769-C-T

39025182-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53380597-C-G

39025419-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53380428-G-C

39025725-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53380140-C-G

http://identifiers.org/hco/13/GRCh38#39025951-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53379782-A-C

39026254-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53379524-T-C

39026268-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53379514-T-C

39026268-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53379514-T-G

39026406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53379376-G-A

39026428-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53379354-A-G

39026444-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53379337-G-T

39026445-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53379336-A-G

39026474-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53379310-G-T

http://identifiers.org/hco/13/GRCh38#39026490-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53379294-C-A

39026490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53379294-C-T

39026491-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53379293-T-A

39026491-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53379293-T-G

39027965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53379155-G-A

39027965-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53379155-G-C

39027966-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53379154-G-C

39028011-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53379115-A-G

39028035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53379091-C-T

39028129-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53379021-A-G

39028131-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53379019-T-C

39028159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53378989-G-A

39028159-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53378989-G-C

39028178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53378969-A-G

39028178-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53378969-A-T

39028191-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53378961-A-G

39028191-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53378961-A-T

39028306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53378857-G-A

39028306-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53378857-G-T

http://identifiers.org/hco/13/GRCh38#39028333-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53378830-C-A

39028366-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53378798-T-C

39029334-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 53377733-G-C

39029406-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53377665-A-G

39029406-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53377665-A-T

http://identifiers.org/hco/13/GRCh38#39029407-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53377664-C-A

39029407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53377664-C-T

39029417-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53377654-T-C

http://identifiers.org/hco/13/GRCh38#39029488-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53377585-A-C

39029488-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53377585-A-G

39029500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53377573-G-A

39029500-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53377573-G-T

39029504-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53377569-A-T

39029553-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53377507-T-A

39031349-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53377190-C-G

http://identifiers.org/hco/13/GRCh38#39031485-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53377037-C-A

39031515-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53377012-T-A

39031647-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53376885-T-C

39031647-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53376885-T-G

39031667-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53376864-T-A

39031667-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53376864-T-C

39031711-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53376820-T-C

http://identifiers.org/hco/13/GRCh38#39031749-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53376784-C-A

39031868-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53376707-G-T

39031888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53376687-G-A

39033842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53374854-C-T

39034000-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53374691-G-T

39034034-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53374674-A-G

39034082-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53374622-A-G

39034109-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53374603-T-C

39034119-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53374598-A-G

39034153-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53374564-T-G

39034252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53374482-G-A

39034252-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53374482-G-T

39034288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53374448-A-G

39034295-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53374441-A-G

39034304-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53374433-T-G

39034321-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53374418-A-G

39034326-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53374413-G-T

39034345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53374397-G-A

39034824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53374108-G-A

39034910-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53374032-G-T

39034967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53373985-G-A

39034992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53373961-C-T

39035042-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53373903-A-G

http://identifiers.org/hco/13/GRCh38#39035166-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53373593-A-C

39035216-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53373557-G-T

39035276-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53373498-T-C

39035336-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53373436-T-G

http://identifiers.org/hco/13/GRCh38#39035471-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53373304-A-C

http://identifiers.org/hco/13/GRCh38#39035609-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53373212-A-C

39035743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53373108-T-C

39035952-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53372901-A-G

39035982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53372872-C-T

39036135-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53372737-T-C

39036135-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53372737-T-G

39036157-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53372716-T-A

39036294-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53372569-T-C

39036448-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53372312-G-C

39036481-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53372280-T-C

39036484-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53372277-T-C

39036541-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53372223-T-C

39036785-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53372084-T-C

39036965-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53371944-A-G

39036975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53371934-C-T

http://identifiers.org/hco/13/GRCh38#39037128-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53371807-A-C

39037128-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53371807-A-G

39037187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53371749-G-A

39037187-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53371749-G-T

39037441-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: 5 prime UTR variant
orthologous variants: 53371497-T-A

39037441-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: 5 prime UTR variant
orthologous variants: 53371497-T-G

39037445-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: 5 prime UTR variant
orthologous variants: 53371493-T-C

39037449-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: 5 prime UTR variant
orthologous variants: 53371489-T-A

39037449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: 5 prime UTR variant
orthologous variants: 53371489-T-C

39037453-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: 5 prime UTR variant
orthologous variants: 53371485-A-G

http://identifiers.org/hco/13/GRCh38#39037457-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53371481-A-C

39037457-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: 5 prime UTR variant
orthologous variants: 53371481-A-G

39037589-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 53371389-G-T

http://identifiers.org/hco/13/GRCh38#39037634-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#53371372-C-A

http://identifiers.org/hco/13/GRCh38#39037801-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53371291-C-A

39037817-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: 5 prime UTR variant
orthologous variants: 53371275-T-G

39037821-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: 5 prime UTR variant
orthologous variants: 53371271-T-C

39037867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 53371224-C-T

39037886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 53371205-G-A

39037886-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 53371205-G-T

39037902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 53371189-C-T

39037914-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 53371177-G-T

39037928-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 53371163-C-G

39037928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 53371163-C-T

39037966-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 53371125-A-T

39038000-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 53371091-A-G

39038075-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: 5 prime UTR variant
orthologous variants: 53371017-G-A

39038075-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: 5 prime UTR variant
orthologous variants: 53371017-G-T

http://identifiers.org/hco/13/GRCh38#39038080-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53371012-C-A

39038080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: 5 prime UTR variant
orthologous variants: 53371012-C-T

http://identifiers.org/hco/13/GRCh38#39038081-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53371011-C-A

39038081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: 5 prime UTR variant
orthologous variants: 53371011-C-T

39038086-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: 5 prime UTR variant
orthologous variants: 53371006-T-C

http://identifiers.org/hco/13/GRCh38#39038088-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20291
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#53371004-C-A