45374215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: 5 prime UTR variant
orthologous variants: 116438070-T-C

http://identifiers.org/hco/10/GRCh38#45374233-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116438045-C-A

45374233-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: 5 prime UTR variant
orthologous variants: 116438045-C-G

45374233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: 5 prime UTR variant
orthologous variants: 116438045-C-T

http://identifiers.org/hco/10/GRCh38#45374260-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116438020-C-A

45374260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: 5 prime UTR variant
orthologous variants: 116438020-C-T

45374262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: 5 prime UTR variant
orthologous variants: 116438018-G-A

45374262-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: 5 prime UTR variant
orthologous variants: 116438018-G-C

45374268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 116438012-G-A

45374268-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 116438012-G-T

http://identifiers.org/hco/10/GRCh38#45374274-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#116437989-C-A

45374274-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 116437989-C-G

45374274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 116437989-C-T

http://identifiers.org/hco/10/GRCh38#45374276-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#116437987-C-A

45374276-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 116437987-C-G

45374276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 116437987-C-T

45374373-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: 5_prime_UTR_variant, missense_variant, undefined
orthologous variants: 116437890-T-C

http://identifiers.org/hco/10/GRCh38#45374391-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: 5_prime_UTR_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#116437872-C-A

45374391-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: 5_prime_UTR_variant, missense_variant, undefined
orthologous variants: 116437872-C-G

45374391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: 5_prime_UTR_variant, synonymous_variant, undefined
orthologous variants: 116437872-C-T

45374397-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 116437866-A-G

http://identifiers.org/hco/10/GRCh38#45374421-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116437842-C-A

45374421-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 116437842-C-G

45374421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 116437842-C-T

45374554-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116437736-T-C

http://identifiers.org/hco/10/GRCh38#45374556-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116437734-C-A

45374556-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116437734-C-G

45374556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116437734-C-T

http://identifiers.org/hco/10/GRCh38#45374561-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116437729-C-A

45374561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116437729-C-T

45374578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116437710-G-A

45374578-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116437710-G-C

45374612-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116437689-G-C

45374689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron_variant, undefined
orthologous variants: 116437613-C-T

45374692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron_variant, undefined
orthologous variants: 116437610-G-A

45374724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116437575-G-A

45374758-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116437552-G-C

45374765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116437545-G-A

45374794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116437509-C-T

45374823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116437489-C-T

45375009-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116437337-C-G

45375151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116437179-C-T

45375202-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116437145-G-A

45375343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116436945-A-G

45375343-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116436945-A-T

45375397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116436907-G-A

45375423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116436882-A-G

45375438-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116436856-A-G

45375446-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116436849-T-C

45375468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116436828-C-T

45375791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116436538-G-A

http://identifiers.org/hco/10/GRCh38#45375883-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116436455-C-A

45375883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116436455-C-T

45375903-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116436435-C-G

45375903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116436435-C-T

45376290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116436075-T-C

45376312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116436053-G-A

45376832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116435613-C-T

http://identifiers.org/hco/10/GRCh38#45376904-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116435550-C-A

45376931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116435524-G-A

45377167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116435357-A-G

45377173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116435351-C-T

45377344-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116435192-T-A

45377344-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116435192-T-C

http://identifiers.org/hco/10/GRCh38#45377451-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116435092-A-C

45377660-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116434911-T-G

45377748-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116434827-C-G

45377748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116434827-C-T

45378470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116433988-G-A

45378489-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116433969-T-C

45378609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116433858-C-T

45378772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116433689-C-T

45379250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116433079-G-A

45379272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116433058-G-A

http://identifiers.org/hco/10/GRCh38#45379279-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116433051-C-A

45379279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116433051-C-T

45379283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116433033-C-T

45379428-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116432889-C-G

45379481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116432845-C-T

45379535-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116432807-A-T

45379582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116432781-C-T

45382085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116431574-G-A

45382286-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116431436-T-C

http://identifiers.org/hco/10/GRCh38#45382344-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116431406-C-A

45382344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116431406-C-T

45382440-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116431316-T-C

http://identifiers.org/hco/10/GRCh38#45382501-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116431256-A-C

45382519-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 116431238-G-T

45382618-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 116431139-A-G

45382762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116430995-G-A

45382762-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116430995-G-T

45382778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116430979-G-A

45382778-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116430979-G-C

45382778-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116430979-G-T

http://identifiers.org/hco/10/GRCh38#45382817-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116430954-C-A

45382817-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116430954-C-G

45382817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116430954-C-T

45383023-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116430763-C-G

45383023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116430763-C-T

http://identifiers.org/hco/10/GRCh38#45383147-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116430636-A-C

45383184-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116430599-T-G

45383450-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116430251-A-G

45383460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116430241-A-G

45383723-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116429500-C-G

http://identifiers.org/hco/10/GRCh38#45383834-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116429363-C-A

45384347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116428788-C-T

45384539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116428610-C-T

45386541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116426595-G-A

http://identifiers.org/hco/10/GRCh38#45387054-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116426109-C-A

45387054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116426109-C-T

45387100-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116426063-T-G

45387178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116425983-C-T

45387233-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116425919-A-G

http://identifiers.org/hco/10/GRCh38#45395790-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116425377-C-A

45395790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116425377-C-T

http://identifiers.org/hco/10/GRCh38#45395857-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116425308-A-C

45395857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, splice_region_variant
orthologous variants: 116425308-A-G

45395857-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: 5_prime_UTR_variant, intron_variant, splice_region_variant, stop_gained
orthologous variants: 116425308-A-T

45395872-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 116425293-G-T

45395941-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116425224-G-T

http://identifiers.org/hco/10/GRCh38#45395958-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116425208-A-C

http://identifiers.org/hco/10/GRCh38#45395963-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116425203-C-A

45395984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116425186-T-C

45395989-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116425181-C-G

45395989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116425181-C-T

45396032-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116425157-T-A

45396032-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116425157-T-C

45396034-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116425155-T-A

http://identifiers.org/hco/10/GRCh38#45396036-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116425153-A-C

45396036-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116425153-A-G

45396036-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116425153-A-T

45396038-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116425151-T-C

45396038-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116425151-T-G

45396107-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116425123-A-G

45396294-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116424961-T-C

45396684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116424538-C-T

45396950-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116424287-T-G

45396989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116424239-A-G

45396989-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116424239-A-T

http://identifiers.org/hco/10/GRCh38#45397867-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116423725-C-A

45397905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116423699-G-A

http://identifiers.org/hco/10/GRCh38#45397916-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116423688-C-A

45397978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116423615-T-C

45397980-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116423613-G-C

45398008-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116423589-T-C

45398013-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116423584-A-G

45398070-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116423522-G-T

http://identifiers.org/hco/10/GRCh38#45398194-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116423409-A-C

45398268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116423336-G-A

45398301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116423271-A-G

45398410-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116423192-A-G

45403894-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116417042-G-C

45403915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116417022-G-A

45404057-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116416886-A-G

45404131-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116416804-T-G

45404285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116416645-C-T

45404425-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116416536-C-G

45404596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116416392-C-T

45404690-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116416201-C-G

45404690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116416201-C-T

45404942-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116415969-A-G

45404960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116415942-G-A

45409649-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116408216-A-T

45409654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116408211-A-G

45409686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116408178-G-A

45409714-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116408150-A-G

45409899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116407977-G-A

45410084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116405900-A-G

http://identifiers.org/hco/10/GRCh38#45410629-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#116405064-A-C

http://identifiers.org/hco/10/GRCh38#45410658-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#116405049-C-A

45411688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116404706-G-A

45411688-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116404706-G-T

45411696-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116404698-C-T

45412056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116404354-T-C

45412225-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: missense variant
orthologous variants: 116404190-A-G

45412393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116403586-C-T

45412412-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116403569-G-C

45412436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116403538-G-A

45412436-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116403538-G-T

http://identifiers.org/hco/10/GRCh38#45412541-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116403435-A-C

45423843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116401380-G-A

45423843-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116401380-G-C

45423890-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116401334-T-C

45423896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116401328-G-A

45423896-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116401328-G-C

45423896-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116401328-G-T

45423948-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116401289-G-C

45423963-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116401274-T-G

45423968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116401269-G-A

45423968-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116401269-G-T

45423994-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116401247-G-C

45424189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116401073-G-A

45424196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116401066-G-A

45424354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116400945-C-T

45424420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116400842-C-T

45424639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116400533-G-A

45424780-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116400421-T-C

45424891-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116400323-T-G

45425040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116400194-C-T

45425049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116400185-G-A

45425049-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116400185-G-C

45425056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116400178-C-T

45425159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116400089-G-A

45425187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116400062-C-T

http://identifiers.org/hco/10/GRCh38#45425224-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116400026-C-A

45425224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116400026-C-T

45425468-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116399811-T-C

45425998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116399309-C-T

45426001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116399306-C-T

45426005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116399305-G-A

45426229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116399179-T-C

45428532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116397447-G-A

45428532-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116397447-G-T

45428583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116397381-A-G

45428607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116397357-G-A

45428811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116397151-G-A

45428811-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116397151-G-T

45428813-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116397149-T-C

http://identifiers.org/hco/10/GRCh38#45428820-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116397121-C-A

45428820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116397121-C-T

45428923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116396986-G-A

45428991-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116396923-T-C

http://identifiers.org/hco/10/GRCh38#45429013-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116396904-C-A

45429013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116396904-C-T

45429037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116396880-C-T

45429547-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116396544-A-T

http://identifiers.org/hco/10/GRCh38#45429847-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116396246-C-A

45429938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116396174-C-T

45429939-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116396173-A-G

45429974-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116396143-A-G

45429987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116396106-C-T

45430077-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116395940-T-G

http://identifiers.org/hco/10/GRCh38#45430175-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116395843-C-A

45433379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116395590-C-T

45439698-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116393128-A-G

45440316-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116392640-G-T

45440323-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116392633-T-C

45440323-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116392633-T-G

45440403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116392562-T-C

45440420-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116392546-A-G

45440616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116392350-G-A

45440616-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116392350-G-C

45440637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116392329-C-T

45440667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116392299-G-A

http://identifiers.org/hco/10/GRCh38#45440709-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116392261-C-A

45440709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116392261-C-T

45440714-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116392256-G-C

45440726-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116392241-G-C

45440726-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116392241-G-T

45440745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116392222-G-A

45440745-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116392222-G-T

45440748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116392220-G-A

45440748-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116392220-G-T

45441068-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116391800-A-G

45441110-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116391764-G-C

http://identifiers.org/hco/10/GRCh38#45441215-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116391685-A-C

45441215-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116391685-A-G

45441215-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116391685-A-T

45441258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116391630-G-A

45441258-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116391630-G-T

45441263-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116391625-G-T

45441264-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116391624-G-C

45441339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 116391573-C-T

http://identifiers.org/hco/10/GRCh38#45442911-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116391007-C-A

45442911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 116391007-C-T

45442952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 116390959-G-A

45442952-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 116390959-G-C

45442952-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 116390959-G-T

45442969-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 116390941-T-A

45442969-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 116390941-T-G

http://identifiers.org/hco/10/GRCh38#45443020-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116390892-C-A

45443020-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 116390892-C-T

45443038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 116390875-G-A

http://identifiers.org/hco/10/GRCh38#45443062-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116390851-C-A

45443062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116390851-C-T

45443092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116390821-G-A

45443104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116390809-G-A

45443104-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116390809-G-T

45443155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116390758-G-A

45443457-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116390481-A-G

45443566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116390335-G-A

45443566-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116390335-G-C

45443566-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116390335-G-T

http://identifiers.org/hco/10/GRCh38#45443595-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116390309-C-A

45443613-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116390280-G-C

45443613-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116390280-G-T

45443628-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116390265-T-C

http://identifiers.org/hco/10/GRCh38#45443751-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116390158-C-A

45443751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116390158-C-T

http://identifiers.org/hco/10/GRCh38#45443840-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116390069-C-A

45443840-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116390069-C-G

45443840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116390069-C-T

45443851-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116390057-G-T

45443874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116390018-G-A

45443874-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116390018-G-T

http://identifiers.org/hco/10/GRCh38#45444009-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116389865-C-A

45444009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116389865-C-T

45444043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116389725-G-A

45444043-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116389725-G-T

http://identifiers.org/hco/10/GRCh38#45444046-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116389722-C-A

45444046-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116389722-C-G

45444046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116389722-C-T

45444058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116389710-G-A

45444069-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116389643-A-G

http://identifiers.org/hco/10/GRCh38#45444137-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116389568-C-A

45444137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116389568-C-T

45444156-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116389549-T-A

45444156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116389549-T-C

45444161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116389544-G-A

45444161-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116389544-G-T

45444301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116389404-G-A

http://identifiers.org/hco/10/GRCh38#45444323-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116389383-C-A

45444323-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116389383-C-G

45444323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116389383-C-T

45444328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116389378-G-A

45444328-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116389378-G-T

http://identifiers.org/hco/10/GRCh38#45444346-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116389360-C-A

45444346-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116389360-C-G

45444346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116389360-C-T

http://identifiers.org/hco/10/GRCh38#45444347-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116389359-C-A

45444425-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116389283-A-G

http://identifiers.org/hco/10/GRCh38#45444440-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116389266-C-A

45444458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116389248-G-A

45444458-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116389248-G-C

45444458-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron variant
orthologous variants: 116389248-G-T

45444629-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 116389045-C-T

45444687-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 116389000-T-C

http://identifiers.org/hco/10/GRCh38#45444690-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116388997-A-C

45444704-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 116388984-A-G

45444705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 116388983-G-A

45444705-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 116388983-G-T

45444709-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 116388979-A-G

45444787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 116388926-G-A

45444787-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 116388926-G-T

http://identifiers.org/hco/10/GRCh38#45445181-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116388688-A-C

45445191-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116388678-G-T

45445202-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116388667-T-C

45445386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116387972-G-A

45445386-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116387972-G-T

45445403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116387949-T-C

http://identifiers.org/hco/10/GRCh38#45445411-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116387941-C-A

45445452-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116387903-T-C

45445466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116387890-T-C

45445467-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116387889-A-G

45445596-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 116387769-T-C

http://identifiers.org/hco/10/GRCh38#45445673-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116387692-A-C

45445673-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 116387692-A-G

45445717-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116387640-C-G

45445759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116387601-G-A

http://identifiers.org/hco/10/GRCh38#45445916-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116387405-C-A

45445916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116387405-C-T

45445929-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 435
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116387392-T-A