16526842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 36303378-T-C

http://identifiers.org/hco/7/GRCh38#16526843-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36303377-A-C

16526852-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 36303368-T-C

16526877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 36303353-A-G

16527840-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36302936-A-T

16528094-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36302707-G-A

http://identifiers.org/hco/7/GRCh38#16528240-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36302573-C-A

http://identifiers.org/hco/7/GRCh38#16528359-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36302471-A-C

16528434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36302388-A-G

16528466-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36302349-A-G

16528860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36301984-C-T

16529249-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36301584-T-C

16529669-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36300214-T-C

16529735-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36300149-G-C

16529869-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36300019-A-G

16530086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36299638-C-T

16530087-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36299625-T-C

http://identifiers.org/hco/7/GRCh38#16530094-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36299619-C-A

16530135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36299529-G-A

http://identifiers.org/hco/7/GRCh38#16530141-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36299523-A-C

16530141-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36299523-A-G

16530182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36299488-C-T

16530201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36299469-T-C

16530236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36299434-G-A

16530236-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36299434-G-T

http://identifiers.org/hco/7/GRCh38#16530281-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36299389-C-A

16530296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36299374-G-A

16530296-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36299374-G-T

16530323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36299347-G-A

16530323-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36299347-G-T

16530362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36299306-G-A

16530371-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36299297-T-A

http://identifiers.org/hco/7/GRCh38#16530386-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36299288-C-A

http://identifiers.org/hco/7/GRCh38#16530409-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36299266-C-A

16530409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36299266-C-T

16530540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36299142-T-C

16530590-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36299093-T-C

16530680-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36299004-A-G

16531240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36298796-C-T

16531513-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36298528-T-C

16531513-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36298528-T-G

16532532-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 36297632-G-C

16532619-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36297517-T-C

16532621-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36297515-T-A

http://identifiers.org/hco/7/GRCh38#16532626-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36297510-A-C

16532642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36297494-A-G

http://identifiers.org/hco/7/GRCh38#16532667-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36297471-C-A

16532682-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36297451-A-G

16532690-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36297437-T-C

16532701-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36297426-T-C

16532701-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36297426-T-G

16532727-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36297402-G-T

http://identifiers.org/hco/7/GRCh38#16532745-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36297384-A-C

16532745-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36297384-A-T

16532772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36297358-G-A

16532772-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36297358-G-T

16532807-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36297347-G-T

16532813-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36297341-T-G

16532820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 36297335-G-A

16532820-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 36297335-G-T

16532884-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36297277-A-T

http://identifiers.org/hco/7/GRCh38#16532935-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36297230-A-C

http://identifiers.org/hco/7/GRCh38#16532937-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36297228-A-C

http://identifiers.org/hco/7/GRCh38#16532942-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36297223-C-A

16532973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36297202-G-A

http://identifiers.org/hco/7/GRCh38#16532990-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36297182-C-A

16533018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36297154-G-A

16533018-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36297154-G-T

16533019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36297153-C-T

16533046-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36297129-T-C

16533059-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36297117-T-G

16533112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36297086-G-A

http://identifiers.org/hco/7/GRCh38#16533253-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36296948-C-A

16533388-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36296849-G-T

16533416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36296819-G-A

16533416-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36296819-G-T

16533421-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36296814-A-G

16533428-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36296807-T-A

http://identifiers.org/hco/7/GRCh38#16533614-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36295454-C-A

16533680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36295386-G-A

16533702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36295362-G-A

16533792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36295193-G-A

16533822-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36295163-T-C

16533972-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36295004-A-T

16534069-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36294930-G-C

16534235-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36294791-G-C

16537302-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36293618-A-G

16537311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36293606-C-T

16537318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36293601-C-T

16537418-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36293527-T-A

16537555-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36293413-T-C

16537574-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 36293394-A-T

http://identifiers.org/hco/7/GRCh38#16537631-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36293335-C-A

16537631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 36293335-C-T

16537706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36293260-T-C

16537736-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36293233-T-C

16537758-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36293218-T-C

http://identifiers.org/hco/7/GRCh38#16537794-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36293183-C-A

16537794-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36293183-C-G

16537794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36293183-C-T

http://identifiers.org/hco/7/GRCh38#16537821-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36293156-C-A

16537821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36293156-C-T

http://identifiers.org/hco/7/GRCh38#16537905-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36293080-C-A

16537940-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36293051-T-C

16538067-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36292976-T-G

16538104-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36292939-A-G

16538121-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36292924-A-G

16541165-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36291863-A-T

http://identifiers.org/hco/7/GRCh38#16541201-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36291827-C-A

16541236-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36291797-T-G

16541252-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36291786-T-C

16541376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36291664-G-A

16541540-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36291502-T-A

16545700-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36290621-T-G

16545817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36290509-C-T

16545988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36290106-G-A

16545988-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36290106-G-T

16546142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36289964-C-T

16549234-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36287979-T-A

16549310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36287909-G-A

16549364-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36287855-T-C

16549373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36287846-A-G

16549500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36287721-C-T

http://identifiers.org/hco/7/GRCh38#16549539-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36287686-C-A

16549541-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36287684-C-T

16549668-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36287579-A-G

16549891-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36287369-T-A

16553136-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36276521-T-A

16553136-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36276521-T-C

16553604-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36276034-T-C

16553640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36275997-C-T

http://identifiers.org/hco/7/GRCh38#16554294-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36275251-C-A

16554308-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36275237-T-G

16554474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36275091-C-T

16554620-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36274967-T-C

16554675-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36274913-T-A

16554854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36274737-G-A

16554854-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36274737-G-T

16555353-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36274270-A-G

http://identifiers.org/hco/7/GRCh38#16555774-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36274205-C-A

http://identifiers.org/hco/7/GRCh38#16557363-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36272825-C-A

16557363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: missense variant
orthologous variants: 36272825-C-T

16557384-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: missense variant
orthologous variants: 36272804-A-G

16557394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: missense variant
orthologous variants: 36272794-G-A

16557394-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: missense variant
orthologous variants: 36272794-G-C

16557394-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: missense variant
orthologous variants: 36272794-G-T

http://identifiers.org/hco/7/GRCh38#16557525-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36272661-A-C

16557525-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36272661-A-G

16557631-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36272571-T-G

16557754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36272424-T-C

16557809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36272370-C-T

16557880-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36272307-T-A

16557880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36272307-T-C

16558023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36272165-G-A

16558113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36272070-A-G

16558143-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36272045-G-C

16558164-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36272016-T-C

16558204-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36271978-A-T

http://identifiers.org/hco/7/GRCh38#16558234-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36271939-C-A

16558709-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36271774-A-G

16558709-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36271774-A-T

16558720-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36271763-T-C

16558757-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36271733-A-T

16558777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36271713-C-T

16558806-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36271684-A-G

http://identifiers.org/hco/7/GRCh38#16558918-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36271569-C-A

16558918-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: missense variant
orthologous variants: 36271569-C-G

16558918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: missense variant
orthologous variants: 36271569-C-T

16559040-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36271443-T-A

16559040-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36271443-T-C

16559041-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36271442-A-G

16559041-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36271442-A-T

http://identifiers.org/hco/7/GRCh38#16559131-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36271426-C-A

16559131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36271426-C-T

http://identifiers.org/hco/7/GRCh38#16559141-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36271416-C-A

16559141-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36271416-C-G

http://identifiers.org/hco/7/GRCh38#16559143-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36271414-C-A

http://identifiers.org/hco/7/GRCh38#16559144-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36271413-A-C

16559144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36271413-A-G

16559420-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36271357-G-T

16559434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36271343-A-G

16559445-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36271339-T-C

16559491-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36271310-T-C

http://identifiers.org/hco/7/GRCh38#16559648-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36271159-C-A

16559671-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36271134-T-A

16559680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36271125-G-A

16559811-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36270991-A-G

16560111-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36270699-A-G

16560176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36270656-A-G

16560304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36270558-C-T

16560322-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36270542-T-A

16560360-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36270507-C-G

16560679-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36270201-A-T

16560706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36270174-G-A

16560706-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36270174-G-T

16560916-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36269986-T-C

16560986-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36269970-A-T

16561032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36269930-C-T

16561039-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36269925-T-A

16561107-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36269852-T-C

16561157-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36269813-T-C

16561334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36269642-G-A

16561471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36269533-G-A

16561483-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36269521-T-C

16561604-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36269389-G-C

16562258-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36268837-C-G

16562349-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36268735-T-C

16562351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36268733-C-T

16562691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36268149-G-A

16562723-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36268125-C-G

16562747-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36268105-T-C

http://identifiers.org/hco/7/GRCh38#16563031-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36267860-C-A

http://identifiers.org/hco/7/GRCh38#16563143-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36267755-A-C

16563325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36267231-G-A

16563335-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36267221-A-G

16563602-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36266953-A-G

16563671-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36266884-T-C

16563707-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36266824-G-C

16563724-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36266807-T-C

16564074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36266213-G-A

16564089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36266192-G-A

16564145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36266143-G-A

16564148-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36266140-A-T

16564202-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36266085-G-T

16564364-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36265944-A-G

16564368-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36265940-C-G

16564389-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36265905-A-G

16564415-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36265879-T-C

16564921-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36265415-T-G

16564930-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36265406-T-G

16564966-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36265366-G-C

16564969-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36265363-T-A

16565445-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36265215-T-A

16565445-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36265215-T-G

16565851-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36264841-T-C

16565855-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36264837-A-G

http://identifiers.org/hco/7/GRCh38#16566090-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36264641-A-C

16566090-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36264641-A-G

16566124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36264612-T-C

16566125-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36264611-G-T

16566151-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36264586-G-T

16566166-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36264567-G-C

16566166-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36264567-G-T

16566224-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36264499-A-G

16566262-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36264462-T-A

16566368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: synonymous variant
orthologous variants: 36264358-C-T

16566405-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36264321-A-G

16566405-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36264321-A-T

http://identifiers.org/hco/7/GRCh38#16566889-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36263309-A-C

16566994-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36263222-T-C

16567015-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36263191-T-C

16567256-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36262978-A-T

16567261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36262973-A-G

16567261-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36262973-A-T

16567284-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36262953-T-A

16567284-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36262953-T-C

16567336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36262769-A-G

16567341-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36262764-T-C

16567370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36262735-A-G

16567383-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 36262722-T-C

16567471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: missense variant
orthologous variants: 36262634-G-A

16567471-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: missense variant
orthologous variants: 36262634-G-C

http://identifiers.org/hco/7/GRCh38#16567546-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36262559-A-C

16567546-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36262559-A-G

16567546-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36262559-A-T

16567581-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36262539-A-G

16567581-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36262539-A-T

16567606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36262514-G-A

16567645-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36262477-A-G

16567663-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36262464-A-G

http://identifiers.org/hco/7/GRCh38#16567689-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36262437-A-C

16567689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36262437-A-G

16567782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36262339-G-A

16567949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36262174-C-T

http://identifiers.org/hco/7/GRCh38#16579297-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36260362-C-A

16579297-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36260362-C-G

16579297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36260362-C-T

16579538-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36260151-A-G

16579577-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36260112-G-T

16579931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36259812-G-A

16579931-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36259812-G-C

16579931-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36259812-G-T

http://identifiers.org/hco/7/GRCh38#16580025-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36259760-C-A

16580025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36259760-C-T

16580090-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: synonymous variant
orthologous variants: 36259699-T-C

16580202-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36259574-A-T

16580302-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36259478-A-T

16580998-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36259114-T-C

16580998-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36259114-T-G

16581312-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36258708-T-A

16581312-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: intron variant
orthologous variants: 36258708-T-C

http://identifiers.org/hco/7/GRCh38#16581340-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36258682-C-A

16581340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: missense variant
orthologous variants: 36258682-C-T

http://identifiers.org/hco/7/GRCh38#16581409-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36258613-A-C

16581409-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: missense variant
orthologous variants: 36258613-A-G

16581424-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: missense variant
orthologous variants: 36258598-G-C

16581460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: missense variant
orthologous variants: 36258562-G-A

16581460-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: missense variant
orthologous variants: 36258562-G-T

http://identifiers.org/hco/7/GRCh38#16581510-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36258514-C-A

16581528-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42972
most severe consequence: 3 prime UTR variant
orthologous variants: 36258496-T-C