5431581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142810653-G-A

5431581-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142810653-G-C

5431581-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142810653-G-T

5431708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142810782-G-A

5435778-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142820612-T-C

5435778-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142820612-T-G

5435935-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142820752-A-G

5436000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142820792-G-A

5436006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142820798-G-A

5436006-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142820798-G-T

5436114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142820884-C-T

http://identifiers.org/hco/7/GRCh38#5446493-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#142824777-A-C

5446502-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142824786-G-C

5446668-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142824943-C-G

5447370-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142825469-G-C

5447427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142825534-A-G

5447478-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142825596-G-C

5447525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142825643-G-A

5447533-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142825651-A-G

5447595-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142825713-A-G

5450317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142827810-G-A

5450356-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142827849-A-G

5450713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142828128-C-T

5450722-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142828139-G-C

5450881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142828304-G-A

5453204-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 142836325-G-C

5453400-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142836480-G-A

5453509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142836583-G-A

5455482-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142840216-T-C

http://identifiers.org/hco/7/GRCh38#5457800-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#142843497-C-A

5457810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 142843507-G-A

5457810-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 142843507-G-T

5458147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142843851-G-A

5458151-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142843855-T-C

5458235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142843947-G-A

5458235-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142843947-G-T

5458251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142843963-C-T

5458253-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142843965-C-G

5458420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142844123-C-T

5458422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142844125-G-A

5458437-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142844136-T-C

5458550-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142844248-T-A

5458711-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142844400-A-G

http://identifiers.org/hco/7/GRCh38#5475754-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#142852661-C-A

5475797-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 142852701-T-C

5475797-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 142852701-T-G

http://identifiers.org/hco/7/GRCh38#5475842-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#142852746-C-A

5475842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 142852746-C-T

http://identifiers.org/hco/7/GRCh38#5475974-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#142852875-A-C

5475974-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 142852875-A-G

5475994-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 142852887-G-C

5475994-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 142852887-G-T

5475995-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 142852888-T-C

5475995-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 142852888-T-G

5476015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 142852908-A-G

http://identifiers.org/hco/7/GRCh38#5476030-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#142852911-C-A

5476030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 142852911-C-T

5476051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 142852923-C-T

5476065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 142852937-G-A

5476065-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 142852937-G-T

5476067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 142852939-G-A

5476070-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 142852942-G-C

5476070-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 142852942-G-T

5476081-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 142852955-T-A

5476081-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 142852955-T-C

5476084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 142852958-G-A

5476084-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 142852958-G-T

5476121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 142852993-G-A

5476121-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 142852993-G-T

5476139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 142853018-G-A

5476139-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 142853018-G-C

5476159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 142853041-G-A

5476159-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 142853041-G-C

5476159-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 142853041-G-T

5476172-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 142853058-A-G

5476187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 142853073-C-T

5476192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 142853078-G-A

5476192-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 142853078-G-T

http://identifiers.org/hco/7/GRCh38#5476209-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#142853110-C-A

http://identifiers.org/hco/7/GRCh38#5476222-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#142853123-C-A

5476222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 142853123-C-T

http://identifiers.org/hco/7/GRCh38#5476227-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#142853131-C-A

http://identifiers.org/hco/7/GRCh38#5476236-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#142853169-C-A

5476236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 142853169-C-T

http://identifiers.org/hco/7/GRCh38#5476283-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#142853214-C-A

5476283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 142853214-C-T

5476322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 142853246-C-T

5477227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 142853514-G-A

5477267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 142853548-C-T

5477299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 142853583-G-A

5477299-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 142853583-G-T

5478762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 142855180-G-A

5478762-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 142855180-G-T

5478770-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 142855192-A-G

http://identifiers.org/hco/7/GRCh38#5478827-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#142855249-C-A

5478827-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 142855249-C-G

http://identifiers.org/hco/7/GRCh38#5478841-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#142855252-C-A

5479231-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 142855634-T-C

5479513-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 142856260-T-C

http://identifiers.org/hco/7/GRCh38#5479580-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#142856331-C-A

5479580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 142856331-C-T

5479622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 142856386-G-A

5479622-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 142856386-G-T

5479733-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 142856470-G-T

5479802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 142856535-G-A

5479834-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 142856558-G-A

5479834-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 142856558-G-T

http://identifiers.org/hco/7/GRCh38#5479841-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#142856565-C-A

5479841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 142856565-C-T

http://identifiers.org/hco/7/GRCh38#5479850-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#142856574-C-A

5479850-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 142856574-C-G

5479850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 142856574-C-T

5479862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 142856585-G-A

5479892-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 142856612-T-G

5479901-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 142856619-A-G

5481060-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 142857420-T-C

5481117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 142857471-A-G

5481158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 142857508-G-A

5481158-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 142857508-G-T

5481196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 142857546-G-A

5481196-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 142857546-G-T

5481223-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 142857583-A-G

http://identifiers.org/hco/7/GRCh38#5481257-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#142857615-C-A

http://identifiers.org/hco/7/GRCh38#5481314-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#142857691-C-A

5481314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 142857691-C-T

5481322-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 142857700-T-C

5481327-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 142857705-T-A

5481327-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 142857705-T-C

5481333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 142857711-G-A

5481333-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 142857711-G-T

5481345-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 142857718-G-T

5481376-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 142857745-T-G

5481412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 142857779-G-A

5481412-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 142857779-G-T

http://identifiers.org/hco/7/GRCh38#5481424-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#142857791-C-A

5481424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 142857791-C-T

5481425-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 142857792-A-G

5481425-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 142857792-A-T

http://identifiers.org/hco/7/GRCh38#5481484-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#142857827-C-A

5481484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 142857827-C-T

5481607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 142857916-G-A

5481607-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 142857916-G-C

5481607-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 142857916-G-T

5481644-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 142857945-A-G

5481728-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 142858025-T-G

5481739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 142858035-G-A

5481739-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 142858035-G-C

5481739-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 142858035-G-T

5481766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 142858108-C-T

5481943-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142858287-A-G

5481964-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142858300-T-A

5481964-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142858300-T-G

5481983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142858319-C-T

5481991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142858321-G-A

5481991-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142858321-G-C

5481991-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142858321-G-T

5486946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142863149-G-A

5486946-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142863149-G-C

5486966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142863169-G-A

http://identifiers.org/hco/7/GRCh38#5487029-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#142863216-C-A

5487029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 142863216-C-T

5487052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 142863234-G-A

5487078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 142863257-T-C

http://identifiers.org/hco/7/GRCh38#5491108-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#142864302-C-A

5491108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142864302-C-T

http://identifiers.org/hco/7/GRCh38#5491128-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#142864320-C-A

http://identifiers.org/hco/7/GRCh38#5491130-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#142864322-A-C

5491130-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142864322-A-G

5491176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142864358-G-A

5491176-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142864358-G-T

5491203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142864385-G-A

5491203-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142864385-G-T

5491206-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142864388-G-T

5491211-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142864393-A-T

5491216-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142864398-A-T

http://identifiers.org/hco/7/GRCh38#5491219-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#142864401-C-A

5491219-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142864401-C-G

5491219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142864401-C-T

5491220-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142864402-A-T

5491221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142864403-C-T

5491253-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 142864435-G-C

5491269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 142864451-G-A

5491269-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 142864451-G-C

5491316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 142864498-G-A

5491316-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 142864498-G-C

5491341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 142864523-G-A

5491341-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 142864523-G-T

5491365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 142864547-G-A

5491365-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 142864547-G-C

5491392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 142864574-G-A

5491392-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, stop_gained
orthologous variants: 142864574-G-T

http://identifiers.org/hco/7/GRCh38#5491404-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#142864586-C-A

5491404-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 142864586-C-G

5491404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 142864586-C-T

5491422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 142864604-G-A

5491422-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 142864604-G-T

http://identifiers.org/hco/7/GRCh38#5491478-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#142864655-C-A

5491478-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142864655-C-G

http://identifiers.org/hco/7/GRCh38#5494738-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#142865214-C-A

5494738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 142865214-C-T

5494744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 142865220-G-A

5494834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142865307-C-T

5494835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142865308-G-A

5494923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 142865387-G-A

5495059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142865495-G-A

5495627-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142865970-A-G

5495627-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142865970-A-T

http://identifiers.org/hco/7/GRCh38#5495689-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#142866028-C-A

5495689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142866028-C-T

http://identifiers.org/hco/7/GRCh38#5495693-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#142866032-C-A

5495693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142866032-C-T

5495766-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142866102-C-G

5495766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142866102-C-T

http://identifiers.org/hco/7/GRCh38#5495784-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#142866122-C-A

5495784-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142866122-C-G

5495784-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142866122-C-T

5495904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 142866220-G-A

5495904-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 142866220-G-T

http://identifiers.org/hco/7/GRCh38#5495936-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#142866250-C-A

5495936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142866250-C-T

5495997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142866309-G-A

5495997-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142866309-G-T

http://identifiers.org/hco/7/GRCh38#5496002-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#142866314-C-A

5496002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142866314-C-T

5496008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142866319-C-T

5496053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142866364-G-A

5496053-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142866364-G-T

5499178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: -T-C

http://identifiers.org/hco/7/GRCh38#5499208-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: -C-A

http://identifiers.org/hco/7/GRCh38#5499237-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: -C-A

5499266-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: -T-C

5499285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: -C-T

http://identifiers.org/hco/7/GRCh38#5500502-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#142871308-C-A

5500502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 142871308-C-T

5500505-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 142871311-C-G

5500505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 142871311-C-T

5500631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 142871437-C-T

5500694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 142871500-G-A

5500694-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 142871500-G-C

5500694-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 142871500-G-T

5500727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 142871533-G-A

5500820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 142871626-G-A

5500820-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 142871626-G-T

5500904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 142871710-G-A

5500904-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 142871710-G-T

5500928-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 142871734-G-T

http://identifiers.org/hco/7/GRCh38#5500952-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#142871758-C-A

5500952-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 142871758-C-G

5500952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 142871758-C-T

5500985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 142871791-G-A

5500985-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 142871791-G-C

5500985-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 142871791-G-T

5501096-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 142871902-C-G

5501096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 142871902-C-T

5501171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 142871977-C-T

http://identifiers.org/hco/7/GRCh38#5501186-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#142871992-C-A

5501186-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 142871992-C-G

5501186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 142871992-C-T

5501216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 142872022-G-A

5501273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 142872079-G-A

5501273-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 142872079-G-T

5501425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 142872231-G-A

5501425-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 142872231-G-C

5501425-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 142872231-G-T

http://identifiers.org/hco/7/GRCh38#5501459-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#142872265-A-C

5501459-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 142872265-A-G

http://identifiers.org/hco/7/GRCh38#5501495-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#142872301-A-C

5501555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 142872361-G-A

5501555-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 142872361-G-T

5501720-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 142872526-G-T

5501759-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 142872565-C-G

5501807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 142872613-G-A

5501807-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 142872613-G-T

5501813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 142872619-G-A

5501813-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 142872619-G-T

http://identifiers.org/hco/7/GRCh38#5501865-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#142872671-C-A

5501865-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 142872671-C-G

5501865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 142872671-C-T

http://identifiers.org/hco/7/GRCh38#5501867-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#142872673-C-A

5501903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 142872709-C-T

5501914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 142872720-G-A

5501914-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 142872720-G-C

5501914-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 142872720-G-T

5501942-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 142872748-G-T

http://identifiers.org/hco/7/GRCh38#5501996-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#142872802-C-A

5501996-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 142872802-C-G

5501997-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 142872803-T-C

http://identifiers.org/hco/7/GRCh38#5502008-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#142872814-C-A

5502008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 142872814-C-T

5502068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142872876-G-A

5502068-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142872876-G-C

5502068-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142872876-G-T

http://identifiers.org/hco/7/GRCh38#5502146-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#142872907-C-A

5502146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142872907-C-T

5502193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142872952-A-G

5502245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142872979-G-A

http://identifiers.org/hco/7/GRCh38#5502279-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#142873009-C-A

5502319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142873063-G-A

5502319-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142873063-G-C

5502396-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142873136-A-G

5502407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142873147-C-T

http://identifiers.org/hco/7/GRCh38#5502500-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#142873235-A-C

5505120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142874151-C-T

http://identifiers.org/hco/7/GRCh38#5505127-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#142874158-C-A

5505233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142874276-C-T

5505260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142874301-T-C

5505267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142874308-A-G

http://identifiers.org/hco/7/GRCh38#5505341-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#142874352-C-A

5505347-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142874358-T-C

5505370-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142874381-G-C

5505370-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142874381-G-T

5505386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142874397-C-T

5505475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 142874487-C-T

5505629-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, splice_region_variant
orthologous variants: 142874629-T-A

5505671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142874724-G-A

5505671-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142874724-G-T

5505687-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142874741-G-C

5505687-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142874741-G-T

5505694-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142874748-G-T

http://identifiers.org/hco/7/GRCh38#5505716-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#142874783-A-C

5505730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142874797-G-A

5505730-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142874797-G-T

5505732-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142874799-A-G

http://identifiers.org/hco/7/GRCh38#5505780-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#142874838-C-A

5505780-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142874838-C-G

5505780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142874838-C-T

5505800-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142874858-T-C

5513004-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142880166-G-C

http://identifiers.org/hco/7/GRCh38#5513059-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#142880219-C-A

5513164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142880317-G-A

5513241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142880365-G-A

5513401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142880577-G-A

5513401-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142880577-G-C

5513532-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142880749-G-T

http://identifiers.org/hco/7/GRCh38#5513543-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#142880761-C-A

5513543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142880761-C-T

5513569-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 142880792-T-A

5513569-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 142880792-T-G

5513606-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 142880828-A-G

5513758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 142880940-G-A

5513758-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 142880940-G-C

5513758-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 142880940-G-T

http://identifiers.org/hco/7/GRCh38#5513785-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#142880967-C-A

5513785-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 142880967-C-G

5513785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21874
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 142880967-C-T