16174720-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: 5 prime UTR variant
orthologous variants: 31751024-G-T

16174862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: 5 prime UTR variant
orthologous variants: 31751159-G-A

16174862-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: 5 prime UTR variant
orthologous variants: 31751159-G-T

http://identifiers.org/hco/3/GRCh38#16174869-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31751166-A-C

16174869-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: 5 prime UTR variant
orthologous variants: 31751166-A-G

http://identifiers.org/hco/3/GRCh38#16174925-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31751199-C-A

16174925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: 5 prime UTR variant
orthologous variants: 31751199-C-T

http://identifiers.org/hco/3/GRCh38#16174995-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31751266-A-C

16175018-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: 5 prime UTR variant
orthologous variants: 31751311-A-G

http://identifiers.org/hco/3/GRCh38#16175072-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31751366-C-A

16175073-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: 5 prime UTR variant
orthologous variants: 31751367-T-C

16175136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: 5 prime UTR variant
orthologous variants: 31751434-G-A

16175136-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: 5 prime UTR variant
orthologous variants: 31751434-G-C

16175262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: synonymous variant
orthologous variants: 31751560-C-T

16175322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: synonymous variant
orthologous variants: 31751620-C-T

16175337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: synonymous variant
orthologous variants: 31751635-G-A

16175373-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: missense variant
orthologous variants: 31751671-G-T

16175518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 31751819-C-T

16175673-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 31751971-C-G

16175673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 31751971-C-T

16175702-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31752000-C-G

16175702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31752000-C-T

16175719-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31752017-T-C

16175722-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31752020-T-A

16175739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31752037-G-A

16175816-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31752128-T-A

16175816-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31752128-T-C

http://identifiers.org/hco/3/GRCh38#16175825-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31752138-C-A

16175825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31752138-C-T

16175826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31752139-A-G

16176193-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31752456-G-T

16176194-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31752457-G-C

http://identifiers.org/hco/3/GRCh38#16176417-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31752678-A-C

16176604-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31752859-T-C

16176631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31752883-C-T

16176701-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31752951-T-G

16176856-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31753120-T-G

http://identifiers.org/hco/3/GRCh38#16177015-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31753259-A-C

16177015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31753259-A-G

16177054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31753284-C-T

16177240-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31753458-A-G

16177438-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31753631-A-G

16177549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31753725-G-A

16177617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31753783-G-A

16177617-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31753783-G-T

16177803-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31753958-G-T

16177837-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31753988-A-G

16177887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31754056-G-A

16177933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31754103-G-A

16177947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31754117-C-T

16178109-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31754271-T-C

16178125-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31754294-T-C

16178155-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31754322-A-G

16178249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31754406-G-A

16178256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31754413-C-T

16178268-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31754422-T-G

16178305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31754459-T-C

16178409-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31754568-G-C

http://identifiers.org/hco/3/GRCh38#16178547-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#31754689-C-A

16178547-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31754689-C-G

16178692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31754751-C-T

16178711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31754770-C-T

16178734-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31754791-A-G

16178871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31754878-G-A

16179072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31755053-C-T

16179401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31755488-G-A

16181461-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31756112-G-C

16181523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31756181-A-G

16181833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31756416-G-A

16181833-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31756416-G-C

16182065-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31756615-T-C

16182106-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31756663-G-T

16182474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31758500-G-A

16182524-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31758539-C-G

16182583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31758593-A-G

16182724-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31758687-A-G

http://identifiers.org/hco/3/GRCh38#16182763-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31758726-C-A

16182763-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31758726-C-G

16182823-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31758784-A-G

16182886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31758828-G-A

http://identifiers.org/hco/3/GRCh38#16182897-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31758840-C-A

16182937-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31758882-A-G

16182953-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31758897-G-T

16183238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31759100-C-T

16183295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31759156-G-A

16183295-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31759156-G-T

16183488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31759334-C-T

16183494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31759340-C-T

http://identifiers.org/hco/3/GRCh38#16183507-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31759353-C-A

16183507-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31759353-C-G

16183507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31759353-C-T

16183515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31759361-G-A

16183543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31759389-G-A

16183620-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31759779-G-T

16183831-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31759967-A-T

16183836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31759972-G-A

16183899-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31760029-A-G

16184088-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31760151-T-C

16184098-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31760161-T-C

16184273-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31760324-T-C

16193675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31761620-C-T

16193690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31761635-C-T

16193873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31761694-G-A

16194011-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31761811-C-G

16194123-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31761937-T-C

16194128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31761941-G-A

16194139-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31761952-T-A

16194150-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31761963-C-G

16194150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31761963-C-T

16195440-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31761988-G-T

16195504-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31762051-A-G

16195517-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31762064-T-C

16195517-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31762064-T-G

16195643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31762175-T-C

16195645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31762177-G-A

16195645-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31762177-G-T

http://identifiers.org/hco/3/GRCh38#16195665-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31762204-C-A

16195665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31762204-C-T

16195666-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31762205-A-G

http://identifiers.org/hco/3/GRCh38#16195675-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31762214-C-A

16195683-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31762222-A-G

16195711-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31762251-T-C

16195736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31762289-G-A

16195738-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31762291-T-C

16195803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 31762356-G-A

16195823-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 31762376-T-C

16195838-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 31762391-T-G

http://identifiers.org/hco/3/GRCh38#16195898-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31762451-C-A

http://identifiers.org/hco/3/GRCh38#16195963-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31762503-C-A

16196001-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31762565-T-C

16196001-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31762565-T-G

16196011-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31762575-A-G

16196078-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31762673-A-G

16196100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31762695-C-T

16196201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31762811-G-A

16196248-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31762865-C-G

16196286-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31762901-A-T

16196488-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31763044-G-C

16196505-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31763061-G-C

http://identifiers.org/hco/3/GRCh38#16196558-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31763115-C-A

16196558-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31763115-C-T

16196567-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31763128-C-G

16196567-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31763128-C-T

16196953-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31764148-A-G

16196967-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31764183-G-T

http://identifiers.org/hco/3/GRCh38#16196968-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31764184-C-A

16197043-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31764259-G-T

16200545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31764971-G-A

16200703-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 31765130-T-A

16200704-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 31765131-C-G

16200722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 31765149-G-A

16200743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 31765170-T-C

16200842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31765272-T-C

http://identifiers.org/hco/3/GRCh38#16200904-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31765338-C-A

16200904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31765338-C-T

http://identifiers.org/hco/3/GRCh38#16200941-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31765380-A-C

16200941-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31765380-A-G

16200941-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31765380-A-T

http://identifiers.org/hco/3/GRCh38#16200959-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31765399-C-A

16201829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31765847-C-T

16201849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31765867-C-T

16201866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31765883-C-T

16201924-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31765955-T-C

16202695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31766262-G-A

16203151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31766572-C-T

16203174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31766593-G-A

16203819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31767591-C-T

16203885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31767678-G-A

16203890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31767686-C-T

16203926-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31767732-G-C

16204068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31767872-G-A

16208364-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31768106-T-C

16208426-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31768175-A-T

16208451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31768203-C-T

16208491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31768242-A-G

16208491-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31768242-A-T

16208587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 31768335-G-A

16208593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 31768341-C-T

16208638-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 31768386-G-T

16209425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron variant
orthologous variants: 31768984-C-T

http://identifiers.org/hco/3/GRCh38#16210972-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31769854-C-A

16210972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron variant
orthologous variants: 31769854-C-T

http://identifiers.org/hco/3/GRCh38#16211008-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31769891-C-A

16211008-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron variant
orthologous variants: 31769891-C-G

http://identifiers.org/hco/3/GRCh38#16211040-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31769923-C-A

http://identifiers.org/hco/3/GRCh38#16211041-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31769924-C-A

16211042-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron variant
orthologous variants: 31769925-A-G

16211048-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron variant
orthologous variants: 31769930-G-C

16211062-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron variant
orthologous variants: 31769942-C-G

16211287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron variant
orthologous variants: 31770164-G-A

16211287-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron variant
orthologous variants: 31770164-G-T

16211335-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron variant
orthologous variants: 31770198-A-G

16211422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron variant
orthologous variants: 31770279-C-T

16211478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron variant
orthologous variants: 31770350-C-T

16211545-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron variant
orthologous variants: 31770415-C-G

16211545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron variant
orthologous variants: 31770415-C-T

16211763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron variant
orthologous variants: 31771057-G-A

16211955-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron variant
orthologous variants: 31771245-A-G

16211955-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron variant
orthologous variants: 31771245-A-T

16212008-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron variant
orthologous variants: 31771302-T-G

16212069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron variant
orthologous variants: 31771348-G-A

16212177-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron variant
orthologous variants: 31771432-A-G

16212305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron variant
orthologous variants: 31771550-C-T

http://identifiers.org/hco/3/GRCh38#16212357-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31771609-C-A

16212433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron variant
orthologous variants: 31771675-G-A

16212433-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron variant
orthologous variants: 31771675-G-T

http://identifiers.org/hco/3/GRCh38#16212443-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31771685-C-A

16212443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron variant
orthologous variants: 31771685-C-T

http://identifiers.org/hco/3/GRCh38#16212451-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31771689-C-A

16212451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron variant
orthologous variants: 31771689-C-T

16212453-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron variant
orthologous variants: 31771691-A-G

16212473-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron variant
orthologous variants: 31771707-T-C

16212473-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron variant
orthologous variants: 31771707-T-G

http://identifiers.org/hco/3/GRCh38#16212484-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31771718-C-A

16212484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron variant
orthologous variants: 31771718-C-T

16212643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: synonymous variant
orthologous variants: 31771853-C-T

http://identifiers.org/hco/3/GRCh38#16212650-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31771860-C-A

16212650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: missense variant
orthologous variants: 31771860-C-T

16212669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: missense variant
orthologous variants: 31771879-C-T

16212751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 31771961-C-T

http://identifiers.org/hco/3/GRCh38#16212753-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31771963-C-A

16212753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 31771963-C-T

http://identifiers.org/hco/3/GRCh38#16212795-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31772002-C-A

16212795-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31772002-C-G

16212795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31772002-C-T

16214856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31773150-G-A

http://identifiers.org/hco/3/GRCh38#16214946-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31773238-C-A

16215044-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31773354-A-G

16218582-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31773769-A-G

16218670-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31773868-T-C

http://identifiers.org/hco/3/GRCh38#16218691-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31773889-A-C

16218691-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31773889-A-G

16218708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31773906-G-A

16219196-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31774053-G-C

16219287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31774136-G-A

16219287-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31774136-G-T

16219301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31774142-G-A

16219301-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31774142-G-C

16219301-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31774142-G-T

http://identifiers.org/hco/3/GRCh38#16219309-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31774150-C-A

16219309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31774150-C-T

http://identifiers.org/hco/3/GRCh38#16219328-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31774177-C-A

16219403-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 31774255-G-C

16219450-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 31774302-G-C

16219633-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31774466-G-T

http://identifiers.org/hco/3/GRCh38#16219661-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31774497-C-A

http://identifiers.org/hco/3/GRCh38#16219665-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31774501-C-A

16219670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31774506-G-A

16219670-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31774506-G-T

16219673-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31774509-T-C

16219677-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31774513-T-A

16219677-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31774513-T-C

16219693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31774529-G-A

16219768-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31774610-A-G

16219768-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31774610-A-T

16219786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31774627-G-A

16219954-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 31774786-A-G

http://identifiers.org/hco/3/GRCh38#16219993-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: http://identifiers.org/mco/14/GRCm39#31774825-C-A

16219993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 31774825-C-T

16220003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 31774835-C-T

16220023-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 31774855-T-A

16220023-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 31774855-T-C

http://identifiers.org/hco/3/GRCh38#16220126-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31774951-C-A

16220126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 31774951-C-T

http://identifiers.org/hco/3/GRCh38#16220144-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31774969-A-C

16220144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 31774969-A-G

http://identifiers.org/hco/3/GRCh38#16220183-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31775008-C-A

http://identifiers.org/hco/3/GRCh38#16220221-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31775038-C-A

16220221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 31775038-C-T

16220235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 31775051-A-G

16220257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron variant
orthologous variants: 31775072-G-A

16220257-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron variant
orthologous variants: 31775072-G-T

16220279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron variant
orthologous variants: 31775094-C-T

16220286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron variant
orthologous variants: 31775101-C-T

16220297-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron variant
orthologous variants: 31775112-A-G

16220305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron variant
orthologous variants: 31775120-T-C

16220366-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron variant
orthologous variants: 31775177-T-C

16220366-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron variant
orthologous variants: 31775177-T-G

http://identifiers.org/hco/3/GRCh38#16220396-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31775204-A-C

16220396-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron variant
orthologous variants: 31775204-A-G

16220493-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron variant
orthologous variants: 31775283-C-G

16222292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron variant
orthologous variants: 31777934-A-G

16222450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron variant
orthologous variants: 31778056-G-A

http://identifiers.org/hco/3/GRCh38#16222493-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31778102-C-A

16222493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron variant
orthologous variants: 31778102-C-T

http://identifiers.org/hco/3/GRCh38#16222494-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31778103-C-A

16222494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron variant
orthologous variants: 31778103-C-T

http://identifiers.org/hco/3/GRCh38#16222495-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31778104-C-A

16222514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron variant
orthologous variants: 31778123-G-A

16222514-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron variant
orthologous variants: 31778123-G-T

http://identifiers.org/hco/3/GRCh38#16222515-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31778124-C-A

16222515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron variant
orthologous variants: 31778124-C-T

http://identifiers.org/hco/3/GRCh38#16222575-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31778182-C-A

16222597-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron variant
orthologous variants: 31778204-C-G

16222597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron variant
orthologous variants: 31778204-C-T

16222653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: synonymous variant
orthologous variants: 31778259-C-T

16222714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: missense variant
orthologous variants: 31778320-G-A

http://identifiers.org/hco/3/GRCh38#16222809-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31778423-C-A

16222809-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron variant
orthologous variants: 31778423-C-G

http://identifiers.org/hco/3/GRCh38#16222812-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31778426-C-A

16222854-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron variant
orthologous variants: 31778482-T-A

16223141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron variant
orthologous variants: 31778897-G-A

http://identifiers.org/hco/3/GRCh38#16226956-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31779717-A-C

16226958-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron variant
orthologous variants: 31779719-T-C

16227038-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron variant
orthologous variants: 31779799-T-C

http://identifiers.org/hco/3/GRCh38#16227228-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31779991-C-A

http://identifiers.org/hco/3/GRCh38#16227233-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31779995-C-A

16227233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron variant
orthologous variants: 31779995-C-T

16227256-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron variant
orthologous variants: 31780020-T-G

http://identifiers.org/hco/3/GRCh38#16227276-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31780039-C-A

16227276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron variant
orthologous variants: 31780039-C-T

16227322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron variant
orthologous variants: 31780081-G-A

16227322-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron variant
orthologous variants: 31780081-G-C

16227371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 31780120-C-T

16227465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, missense_variant
orthologous variants: 31780214-C-T

http://identifiers.org/hco/3/GRCh38#16227590-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31780317-C-A

16227633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 31780359-T-C

16227642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 31780393-A-G

16227673-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 31780421-T-C

16227673-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 31780421-T-G

16227716-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 31780639-A-G

http://identifiers.org/hco/3/GRCh38#16227721-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31780643-A-C

16227721-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 31780643-A-T

16227818-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 31780770-G-T

16227894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 31780838-G-A

16227894-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 31780838-G-T

http://identifiers.org/hco/3/GRCh38#16227913-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31780857-C-A

16227913-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 31780857-C-G

http://identifiers.org/hco/3/GRCh38#16228038-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31780980-C-A

16228068-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 31781010-T-G

16228109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 31781052-G-A

16228153-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 31781093-A-T

16228269-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 31781172-A-G

http://identifiers.org/hco/3/GRCh38#16228271-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31781174-C-A

16228271-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 31781174-C-G

16228271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 31781174-C-T

16228916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 31781472-G-A

16228916-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 31781472-G-T

16228984-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 31781498-A-G

http://identifiers.org/hco/3/GRCh38#16229008-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31781520-C-A

16229034-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 31781544-T-C

16229173-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 31781656-T-C

16229283-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 31781749-T-C

16229283-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 31781749-T-G

16229288-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 31781754-G-T

http://identifiers.org/hco/3/GRCh38#16229306-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31781772-C-A

http://identifiers.org/hco/3/GRCh38#16229529-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31781984-C-A

16229529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 31781984-C-T

16229544-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 31781999-T-A

16229579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 31782035-G-A

16229579-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 31782035-G-T

16229589-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 31782045-A-G

16229609-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 31782065-T-G

16229639-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 31782091-T-A

16229682-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 31782133-T-C

16229808-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 31782252-A-G

16229972-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 31782415-G-T

16230036-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 31782447-A-G

16230057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 31782468-G-A

16230436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron variant
orthologous variants: 31782816-G-A

16230436-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron variant
orthologous variants: 31782816-G-C

16230464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron variant
orthologous variants: 31782844-G-A

16230568-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron variant
orthologous variants: 31782931-T-A

16230585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron variant
orthologous variants: 31782948-A-G

16231810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 31783225-C-T

16231881-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 31783278-T-C

16231921-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 31783305-A-G

http://identifiers.org/hco/3/GRCh38#16231924-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31783308-C-A

http://identifiers.org/hco/3/GRCh38#16231959-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31783349-A-C

16231959-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 31783349-A-G

http://identifiers.org/hco/3/GRCh38#16232019-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31783409-C-A

http://identifiers.org/hco/3/GRCh38#16232029-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31783419-C-A

16232029-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron variant
orthologous variants: 31783419-C-G

16232218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron variant
orthologous variants: 31783628-C-T

16232274-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21531
most severe consequence: intron variant
orthologous variants: 31783674-G-C